Work schedule standard (mon-fri) environmental conditions office job description are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? thermo fisher scientific inc. is seeki...
Manager/senior manager regulatory affairs join to apply for the manager/senior manager regulatory affairs role at thermo fisher scientific manager/senior manager regulatory affairs 1 day ago be among the first 25 applicants join to apply for the mana...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: • responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with ...
Work schedule standard (mon-fri) environmental conditions office job description are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? thermofisher scientific inc. is seeking an individual with a track record of success in vendor management to join our world-class team of researchers. as a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. responsibilities: 1. collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies. 2. manage vendor relationships and contracts, ensuring flawless execution and delivery. 3. conduct market research and competitive analysis to identify potential vendors. 4. develop and implement vendor performance metrics and conduct regular evaluations. 5. drive continuous improvement initiatives to optimize vendor management processes. requirements: 1. bachelor's degree in business administration or related field, or equivalent experience in the industry. 2. previous experience in vendor management or procurement. 3. strong analytical and negotiation skills. 4. excellent communication and interpersonal skills. 5. proven ability to successfully implement vendor management strategies. at thermofisher scientific, we value diversity and inclusivity. we believe that collaboration and different perspectives drive innovation and lead to exceptional results. we are an equal opportunity employer and strictly prohibit discrimination based on...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. essential functions 1. receives, prepares and submits safety reports to applicable parties. 2. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis. 3. leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines. 4. provides input and feedback to aid the development of program and departmental procedural documents. 5. shares ideas and suggestions with team members. 6. takes an active role in the development and implementation of ideas and suggestions. 7. liaises with relevant departments around safety reporting tasks and attends vario...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff. a day in the life: •provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems with project allocation. •resp...
Work schedule standard (mon-fri) environmental conditions office job description essential functions and other job information receives, prepares and submits safety reports to applicable parties. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis. leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines. provides input and feedback to aid the development of program and departmental procedural documents. shares ideas and suggestions with team members. takes an active role in the development and implementation of ideas and suggestions. liaises with relevant departments around safety reporting tasks and attends various meetings as required. provides input, feedback and guidance to other team members and mentors newstarters. produces metrics and has some involvement in financial project. qualifications: education and experience: bachelor's degree or equivalent and relevant formal academic / vocational qualification. previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to5+ years’). working conditions and environment: work is performed in an office/ laboratory and/or a clinical environment. exposure to biological fluids with potential exposure to infectious organisms. exposure to electrical office equipment. personal protective equipment required such as protective eyewear, garments and glove #j-18808-ljbffr...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.our detailed, goal-oriented pharmacovigilance colleagues manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring.as part of your work with beginning-to-end trial experience, you will expand your knowledge and experience working on clinical trials through every stage of drug development. this includes management and oversight of all contracted services.discover impactful work:as a safety reporting specialist, you will be responsible for receipt, submission, and subsequent tracking of expedited and periodic safety reports pertaining to the department’s projects. you will assi...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.discover impactful work:provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff.a day in the life:• provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems with project allocation.• responsible fo...
Work schedule standard (mon-fri) environmental conditions office el especialista de aplicaciones en campo promueve el soporte científico en las áreas de biología celular y molecular a clientes, vendedores y representantes. además, brinda entrenamiento sobre los productos e instrumentos de thermo fisher scientific orientado en la satisfacción del cliente. principales responsabilidades: brindar soporte y entrenamiento, asistencia técnica, estandarización de protocolos, participación de eventos de marketing, apoyo en demostraciones de producto y resolución de problemas a los usuarios de los productos de thermo fisher. proporcionar informaciones sobre el mercado a través de oportunidades para apoyar el desarrollo de las estrategias de venta, además de actuar en actividades secundarias internas y externas administrando entrenamientos, participando de congresos (como orador, inclusive) y atendiendo en campo para aclarar dudas sobre aplicaciones y para resolver problemas con el uso de productos thermo fisher scientific. apoyo en la orientación al cliente en la elección del mejor producto y metodología, buscando el atendimiento de sus necesidades y la promoción de los productos del portafolio de thermofisher; participar de eventos comerciales y científicos donde thermofisher sea patrocinadora, aclarando dudas, analizando posibilidades de aplicación de soluciones y divulgando los productos y servicios del portafolio de la compañía. asumir responsabilidades operativas y desarrollarse en áreas de negocios corporativos a fin de viabilizar el crecimiento sustentable del d...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.our detailed, goal-oriented pharmacovigilance colleagues manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring.as part of your work with beginning-to-end trial experience, you will expand your knowledge and experience working on clinical trials through every stage of drug development. this includes management and oversight of all contracted services.discover impactful work:as a safety reporting specialist, you will be responsible for receipt, submission, and subsequent tracking of expedited and periodic safety reports pertaining to the department’s projects. you will assist manage...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.discover impactful work:provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff.a day in the life:• provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems with project allocation.• responsible for extract...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. essential functions receives, prepares and submits safety reports to applicable parties. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis. leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines. provides input and feedback to aid the development of program and departmental procedural documents. shares ideas and suggestions with team members. takes an active role in the development and implementation of ideas and suggestions. liaises with relevant departments around safety reporting tasks and attends various meetings a...
**work schedule** standard (mon-fri) **environmental conditions** office at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. essential functions receives, prepares and submits safety reports to applicable parties. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis.leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines.provides input and feedback to aid the development of program and departmental procedural documents.shares ideas and suggestions with team members. takes an active role in the development and implementation of ideas and suggestions.liaises with relevant departments around safety reporting tasks and attends various meetings as required.provides input, feedb...
**actividades**: coordinar y dar cumplimiento a las actividades relacionadas con los proyectos a nível local. esto implica realizar, verificar, asesorar, documentar, generar reportes y mantener el flujo de comunicación dentro del equipo del proyecto para los procesos de recepción, almacenamiento, preparación y embalado de envíos, despacho, devolución, etiquetado/re-etiquetado, reconciliación y destrucción de medicamentos y de suministros clínicos. revisar e implementar los procesos de operaciones logísticas y de control de gestión operativa del establecimiento tercerista contratado por fisher clinical services. estas actividades se realizarán siguiendo las buenas prácticas de fabricación, almacenamiento y distribución, minimizando la cantidad de desvíos en calidad. todas estas operaciones logísticas deberán ser llevadas a cabo de acuerdo a las especificaciones, procedimientos, instrucciones y herramientas informáticas/administrativas requeridas por la compañía y/o cliente. **requisitos básicos mínimos**: - conocimientos de normas gmp, bioseguridad, regulaciones locales y sops. - paquete microsoft office. **evaluación de excel intermedio.**: - experiência en actividad logística y almacenamiento en productos farmacéuticos. **educación/experiência**: - graduados en áreas de la salud, ingeniería, operaciones logísticas, administración. - experiência de hasta **2/3 años en tareas similares en industria farmacéutica, cros, o compañías similares de logística.** idiomas**:inglés oral y escrito nível intermedio-se evaluará escritura.** **habilidades y/o competencia...
Work schedule standard (mon-fri) environmental conditions office job description are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? thermo fisher scientific inc. is seeking an individual with a track record of success in vendor management to join our world-class team of researchers. as a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. responsibilities: - collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies. - manage vendor relationships and contracts, ensuring flawless execution and delivery. - conduct market research and competitive analysis to identify potential vendors. - develop and implement vendor performance metrics and conduct regular evaluations. - drive continuous improvement initiatives to optimize vendor management processes. requirements: - bachelor's degree in business administration or related field, or equivalent experience in the industry. - previous experience in vendor management or procurement. - strong analytical and negotiation skills. - excellent communication and interpersonal skills. - proven ability to successfully implement vendor management strategies. at thermo fisher scientific, we value diversity and inclusivity. we believe that collaboration and different perspectives drive innovation and lead to exceptional results. we are an equal opportunity employer and strictly prohibit discrimination based on race, c...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. essential functions - receives, prepares and submits safety reports to applicable parties. - ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis. - leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines. - provides input and feedback to aid the development of program and departmental procedural documents. - shares ideas and suggestions with team members. - takes an active role in the development and implementation of ideas and suggestions. - liaises with relevant departments around safety reporting tasks and attends various meet...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff.a day in the life:• provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems with project allocation.• responsible ...
We are currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department. this is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. in this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (phase 1 to 4) clinical trials, studies and projects. you will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance. you will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients. you will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. you will also arrange, lead, and report on client and regulatory agency meetings. the following skills are required to be successful in this position: - preparation and assembly of global regulatory submissions - interacting with sponsors, - review and assess clinical trial regulatory documents, - review and assess scientific literature. - manages project teams and preparation - participate in launch meetings, review meetings and project team meetings. optional skills: - experience with bid defense meetings **qualifications - external** what the role requir...
We are currently seeking a regulatory affairs specialist to join our global regulatory affairs department. this is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. in this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (phase 1 to 4) clinical trials, studies and projects. you will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance. you will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients. you will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. you will also arrange, lead, and report on client and regulatory agency meetings. the following skills are required to be successful in this position: - preparation and assembly of global regulatory submissions - interacting with sponsors, - review and assess clinical trial regulatory documents, - review and assess scientific literature. - manages project teams and preparation - participate in launch meetings, review meetings and project team meetings. optional skills: - experience with bid defense meetings **qualifications - external** what the role requires you ...
**summarized purpose**: provides administrative and technical support to project team including planning, organizing and coordinating responsibilities of project administration. maintains procedures, guidelines and documentation. ensures appropriate maintenance of project records and that all regulatory documents are correct, processed and approved. completes data entry and maintenance of data base repositories. assists in preparation or creation of reports and completes data collection for analysis. completes quality review and demonstrates audit readiness. **essential functions and other job information** - completes review, coordination and compilation of files and other materials. distributes project documents and supplies. - processes and tracks local regulatory, study specific or department documents. - performs file review. organizes and maintains correspondence files and other departmental records. analyzes and reconciles project documents, metrics and findings reports within specified timelines. - provides clarification and resolution of findings related to documentation. - may assist with translation materials and translation qc upon request. - composes, copies and distributes communications, reports, documents and forms. performs mass mailings and communications. - maintains vendor trackers. - provides accesses to company, client and vendor systems. - processes local payments (translations, ec/iec, other local vendors, etc.) - assists on project management ad-hoc activities, producing reports or on study plan edition. - coordinates team conf...
Ppd’s (a part of thermo fisher scientific) mission is to improve health. it starts as an idea to find a cure. it becomes a life saved. all in-between, it’s you! we know that meaningful results not only require the right approach, but also the right people. we invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. our project delivery team directs, coordinates and leads the technical and operational aspects of projects, securing the successful completion of clinical trials. the team is therapeutically aligned to respond better to our customer needs. the therapeutic scope includes general medicine, hematology and oncology (hemonc), infectious and respiratory diseases (ird), cardiovascular, metabolic and critical care (cvmet), neuroscience, vaccines and fsp/client-dedicated. as a clinical team manager (ctm), you combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changingtherapies to market. you take ownership, anticipate problems, find solutions and deliver results. you take ownership, anticipate problems, find solutions and deliver results; coordinating the activities of clinical management members which are allocated to a project on a regional or country basis. you will work in partnership with the project manager to ensure the necessary training, tracking and quality systems are in place for the clinical management team and be primarily responsible for the clinical deliverables of the project within agreed timelines and budget. clinical team managers p...
We are looking for a research associate iii (senior health economist - heor) to implement simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. manage multiple projects with tasks varying to degree by project. responsible for assisting the principal investigator with project management scoping, tracking progress, and delegating tasks to the project teams working on multiple projects. you will also: - implement one or more of the following with guidance from the principal investigator: - design and development of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. - program the models using microsoft excel with visual basic for applications (vba) or simulation specialized software (e.g., arena) and conduct model validations. - conduct literature reviews with emphasis on extracting data pertinent to health economic evaluations and cost-effectiveness analyses. - conduct basic statistical analyses (e.g., descriptive statistics and regression analysis) - support development and maintenance of scientific resources (e.g., model templates, modeling training manuals). - draft project deliverables (e.g., excel with vba based models, user guides, model specifications and technical reports) and draft abstracts and sections of manuscripts with possible co-authorship. - responsible for developing a project plan and monitoring project progress (budget, timelines an...
We are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust. as a manager clinical data management, you will help ensure the success of your team and cdm projects. you will work to provide training, mentorship and guideance. this includes but not limited to interviewing new staff, performance management, reviewing and approving time and expense reports. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: manages project staff and workload of direct reports. responsible for training, mentoring, and guiding project staff and direct reports within a portfolio. essential functions: - manages staff, which may include int...
And long-term disability, and volunteer time off in accordance with company policy - retirement and savings programs, such as our competitive 401(k) u.s. retirement savings plan...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. **location/division specific information**: our project delivery colleagues within ppd® clinical research services direct, coordinate and lead the technical and operational aspects of projects, securing the successful completion of clinical trials. through our diverse team, our members engage in variety of initiatives and projects, or are part of global project teams gaining cross-cultural experience. therapeutic scope include**:the therapeutic scope includes general medicine**-** dermatology, gi, (uc/cd), cardiovascular, liver, nephrology, immunology, rare disease, diabetes, obesity, dyslipidemia, women's health, rheumatology, (ra, sle, gout) **discover impactful work**: the (sr.) clinical team manager (ctm) combines deep knowledge, therapeutic expertise, and robust tools to he...
Work schedule standard (mon-fri) environmental conditions office job description thermo fisher scientific offers impactful work globally, enabling customers to improve health and safety. we have a vacancy for a senior icf medical writing project mana...
Work schedule standard (mon-fri) environmental conditions office job description the senior key account manager (kam) for human identification (hid) at thermo fisher scientific has a range of responsibilities, including: customer relations: developin...
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