488 Results for

Senior Research Jobs in Center Valley, PA

Jobs

New!

Allentown, PA6 days ago

$95,000–$130,000 Per Year

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New!

Fort Washington, PA6 days ago

$85,000–$120,000 Per Year

Immediate hire, someone who want to have flexibility to work some days from home, earn a high income, and develop their careers down the management path, work is important but not everything in life we are looking for people attracted to our culture who want to be here for the long term! Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.

Blue Bell, PA8 days ago

Remote

$145,000–$180,000 Per Year

strong>Leads all aspects of Market Access actions in North America

Works cross-functionally with Clinical Affairs, Regulatory Affairs, Governmental Affairs, Commercial, Medical Affairs and Regional Marketing colleagues in North America.
The ideal candidate has owned the market access role during a product launch in the US market and has worked in close collaboration with other business functions (medical affairs, governmental affairs, legal, regulatory, marketing and sales) in prior roles.

Allentown, PA30+ days ago

Full-time

Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care..

Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.

Bethlehem, PA9 days ago

Full-time

Collegeville, Pennsylvania30+ days ago

p>Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. 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.

Blue Bell, PA30+ days ago

Remote

Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

North Wales, PA30+ days ago

$282,200–$444,200 Per Year

Through clinical trials we ensure that our existing and pipeline products are developed to produce safe, effective, and innovative medicines, and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global Policy to ensure timely access to our medicines. Establishing communications with prominent clinical investigators in their particular field of interest, particularly those scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs.

North Wales, PA10 days ago

$282,200–$444,200 Per Year

li>Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs;

Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and.

North Wales, PA30+ days ago

$282,200–$444,200 Per Year

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

Required Skills:

Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.

North Wales, PA15 days ago

$282,200–$444,200 Per Year

li>Assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies.

North Wales, PA30+ days ago

$282,200–$444,200 Per Year

Required Skills: Clinical Development, Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Sciences, Clinical Trial Development, Clinical Trials, Drug Development, Intellectual Curiosity, Oncology, Oncology Research, Pharmaceutical Development, Strategic Planning. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area.

PA30+ days ago

$282,200–$444,200 Per Year

p>The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.

New!

Blue Bell, PA5 days ago

p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

CA30+ days ago

$110,520–$138,150 Per Year

li>

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Bonus, Com, Stock, Benefits & Disclaimer verbiage:

Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level.

New!

West Point, PA4 days ago

$117,000–$184,200 Per Year

p>Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts.

Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.

New!

Spring House, PA4 days ago

p>Required Skills:

Preferred Skills:

Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Collaboration, Data Synthesis, Drug Discovery Development, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Program Management, Scientific Research, Tactical Planning, Technical Credibility.

Building trusted cross‑functional partnerships and influencing decision‑making across Therapeutics Discovery (TD), Preclinical Sciences & Translational Safety (PSTS), Therapeutic Areas (TAs), and TDS in matrixed governance and technical forums.

New!

Spring House, Pennsylvania5 days ago

If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

West Point, PA15 days ago

$117,000–$184,200 Per Year

p>Required Skills:

Automation Systems, Computer Engineering, Computer Science, Data Modeling, Design Applications, Information Technology (IT) Services, Java (Programming Language), Laboratory Automation, Laboratory Safety, Managing Engineering Teams, Market Trends, Oracle Database, Product Development, Release Management, Requirements Management, Robot Framework, Robotics Programming, Sample Management, Software Applications, Solution Architecture, SQL Databases, System Designs, System Integration.

Develop and employ robust software capabilities that empower the creation, renewal, update, and destruction of data, adhering to stringent objectives regarding security, compliance, policy, scalability, efficiency, reliability, fidelity, flexibility, and portability.

Phillipsburg, NJ30+ days ago

$120,000–$140,000 Per Year

p>Directly manage and develop project managers and contributors while leading and influencing indirect reports and cross-functional team members; establish clear expectations, coach teams through complex problem solving, and foster accountability, rigor, and momentum without relying solely on formal authority.

Translate strategic intent into structured, executable plans by defining clear objectives, success metrics, priorities, and milestones, and continuously refining scope and approach based on data, field insights, and close partnership with your direct manager and senior leaders.

New!

PA4 days ago

Remote

About the Business Unit:

M3 Global Research, part of M3 Inc., provides the most comprehensive and highest quality market research recruitment and support services available to the industry with relationships reaching respondents in more than 70 countries worldwide.

Fort Washington, PA30+ days ago

Remote

M3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors. M3 Global Research maintains ISO 20252 and 27001 certifications with the highest quality data collection and project management capabilities that cover the spectrum of quantitative and qualitative techniques utilized today.

West Point, PA20 days ago

$210,400–$331,100 Per Year

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. The Senior Principal Scientist leads a team of health economists to develop and implement health economics and modeling strategies that enable the Company to understand and communicate the full economic value of the Company's oncology products to payers, health technology agencies, policy makers, and other decision-makers in order to optimize market access and patient outcomes.

PA30+ days ago

Remote

p>M3 Global Research maintains ISO 26362 and 27001 certifications with the highest quality data collection and project management capabilities that cover the spectrum of quantitative and qualitative techniques utilized today.

About the Business Unit:

Fort Washington, PA30+ days ago

Remote

M3 Global Research maintains ISO 26362 and 27001 certifications with the highest quality data collection and project management capabilities that cover the spectrum of quantitative and qualitative techniques utilized today. M3 Global Research, part of M3 Inc., provides the most comprehensive and highest quality market research recruitment and support services available to the industry with relationships reaching respondents in more than 70 countries worldwide.

Blue Bell, PA30+ days ago

p>Our benefits examples include:

• Various annual leave entitlements • A range of health insurance offerings to suit you and your family's needs • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

PA30+ days ago

$310,900–$489,400 Per Year

li>

Working closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility.

Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.

North Wales, PA30+ days ago

$310,900–$489,400 Per Year

li>

New!

West Point, PA3 days ago

$142,400–$224,100 Per Year

p>Translational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients.

Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.

Spring House, PA10 days ago

Remote

$58–$58.81 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. The Real-World Evidence (RWE) team within Johnson & Johnson Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.

PA30+ days ago

$255,800–$402,700 Per Year

p>The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.
The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.

North Wales, PA30+ days ago

$255,800–$402,700 Per Year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

Spring House, PA10 days ago

Remote

$55–$58.39 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. The Real-World Evidence (RWE) team within Pharmaceutical Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.

Spring House, PA10 days ago

Remote

$58–$59 Per Hour

This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Horsham, PA30+ days ago

$137,000–$235,750 Per Year

p>Required Skills:

Preferred Skills:

Analytics Dashboards, Clinical Research and Regulations, Clinical Trials, Consulting, Customer Centricity, Data-Driven Decision Making, Digital Culture, Digital Literacy, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Knowledge, Relationship Building, Research and Development, Strategic Thinking, Tactical Planning, Technical Credibility.

Responds in a timely manner to unsolicited scientific inquiries of HCPs/investigators/health care systems/academic medical centers and population health decision makers integrating scientific data including real world evidence into real life practice to meet customer needs.

Blue Bell, PA30+ days ago

Remote

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

PA30+ days ago

Remote

PA30+ days ago

$310,900–$489,400 Per Year

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, medical affairs, and manufacturing to manage clinical development projects; and assist the Section Head in ensuring that appropriate Corporate personnel is informed of the progress of studies of our company and competitors drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility.

Must have experience in industry in the field of Thoracic Oncology Minimum of 3 years of clinical medicine experience Minimum of 5 years of industry experience in drug development Demonstrated record of scientific scholarship and achievement A proven track record in clinical medicine and background in biomedical research is essential Strong interpersonal skills, as well as the ability to function in a team environment, are essential.

New!

Collegeville, PA6 days ago

$284,625–$474,375 Per Year

p>GSK is seeking a highly skilled Senior Medical Director, Clinical Development, Neurodegeneration to provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on neurodegenerative disease including Alzheimer's Dementia (AD).

Key Responsibilities:

Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT).

Blue Bell, PA30+ days ago

li>

Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary.

The Sr LTM will manage and oversee the following throughout the study:

Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.

Horsham, PA16 days ago

$137,000–$235,750 Per Year

The Senior MSL is also responsible for staying abreast of current scientific and treatment landscape trends in the relevant therapeutic areas by critically evaluating the quality, relevance, and applicability of emerging data and provide appropriate scientific support for investigator‑initiated studies, including facilitating scientific exchange and connecting investigators with internal research and grant processes, in accordance with applicable policies and without assuming sponsor responsibilities. The Senior MSL is responsible for developing and enhancing professional relationships with Key thought leaders and health care provider teams, providing fair balanced, objective, non-promotional scientific information, and education to health care professionals and to internal partners through meaningful, evidence based scientific exchange as required by scientific and business needs.

Blue Bell, PA17 days ago

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical program. What You Will Do: Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.

PA30+ days ago

li>

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.

Blue Bell, PA30+ days ago

Remote

ul>

Lead strategic Hepatology drug development program design, delivering tailored, asset-focused solutions across liver diseases including MASLD/MASH, alcohol-associated liver disease (ALD), cirrhosis, viral hepatitis, and other chronic and rare liver conditions like PBC, PSC, PFIC.

Strong understanding of Hepatology clinical trial design, biomarkers, endpoints (e.g., fibrosis staging, histologic and non-invasive markers), and evolving therapeutic landscapes (e.g., MASLD/MASH, alcohol-associated liver disease (ALD), cirrhosis, immuno-Hepatology approaches and antiviral therapies).

Collegeville, PA17 days ago

Pipeline Project Managers compose a community of drug development experts applying industry-leading project management practices to plan and deliver pipeline projects with industry-leading performance: Apply a holistic perspective and broad knowledge of drug discovery (pre-clinical) to help Research teams test ideas and optimize the strategy. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.

Collegeville, PA30+ days ago

$284,250–$473,750 Per Year

Robust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution Highly developed communication and interpersonal skills appropriate to the target audience and senior stakeholders, promoting effective decision-making in a highly matrixed environment Demonstrated track record of quality decision-making and innovative problem resolution in critical situations Knowledge of regulatory requirements to support registration, including knowledge and adherence to GCP principles. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.

Collegeville, PA30+ days ago

$214,900–$358,100 Per Year

Provides clinical guidance to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends; reviews and queries data; presents data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical guidance to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and ensures clinical documents are updated in response to emerging safety profile; tracks and reconciles Serious Adverse Events; leads clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.

Blue Bell, PA11 days ago

li>

Collaborating with cross-functional teams to assess supply needs, develop strategies, and ensure alignment with study timelines and regulatory requirements.

As a Senior Clinical Supplies Specialist at ICON, you will manage and coordinate clinical supplies activities to support the successful execution of clinical trials.

PA18 days ago

This role manages study timelines, budgets, vendors, and operational deliverables while coordinating cross-functional study teams in a hub-and-spoke model to ensure efficient study execution.

Serve as the central hub for the study core team, coordinating activities across Clinical Strategy, Data Management, Biometrics, Monitoring, Site Management, Data Systems, and Clinical Trial Associates.

Bethlehem, PA30+ days ago

Remote

$68,970–$113,310 Per Year

p>The Senior RN Clinical Consultant will work in partnership with Clinical and Vocational Leaders to provide ongoing coaching and oversight to Clinical Consultants and will serve as clinical subject matter expert in all lines of business (STD/LTD/Appeals) and products, action planning management, and Guardian systems. They will assist the Clinical Team Manager in managing and resolving issues that come up related to clinical processes, claim management activities, customer inquiries, and quality.

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Senior Research Jobs in Center Valley, PA

Senior Advisory Accountant (Hybrid) Jobot

Tax Senior Jobot

Sr Manager, Market Access - US - Medical Device Joulé

Clinical Research Coordinator I- Precision Medicine St. Luke's Health Network, Inc.

Clinical Research Coordinator I (PA/NJ residents only) St. Luke's Health Network, Inc.

FSP Senior Research Scientist-Dissolution Method Development Thermo Fisher Scientific

Senior Clinical Research Associate ICON Plc

Senior Director, Clinical Research Merck & Co Inc

Senior Principal Scientist, Clinical Research, Breast Cancer Merck & Co Inc

Senior Principal Scientist, Clinical Research, Immunology Merck & Co Inc

Senior Principal Scientist, Clinical Research, GI Merck & Co Inc

Senior Clinical Director (Senior Principal Scientist), Clinical Research, RCC Merck & Co Inc

Senior Clinical Director, Clinical Research, Hematology Merck & Co Inc

Senior Clinical Research Associate - East Coast ICON Plc

Sr. Clinical Research Associate ICON Plc

Senior Scientist, Clinical Research Merck & Co Inc

Senior Principal Scientist, Biologics Discovery Process Research Integrator Johnson & Johnson

Senior Principal Scientist, Biologics Discovery Process Research Integrator 6084-Janssen Research & Development Legal Entity

Sr. Specialist, Research Automation Systems Integrator Merck & Co Inc

Senior Project Manager, Research & Development Oishii Farm Corp

Senior Account Manager - Market Research (Remote) M3 USA Corp

Senior Account Manager - Market Research (Remote) M3 Global Research (US)

Senior Principal Scientist, Outcomes Research Merck & Co Inc

Senior Qualitative Project Manager, Market Research (Remote) M3 USA Corp

Senior Qualitative Project Manager, Market Research (Remote) M3 Global Research (US)

Clinical Research Associate ICON Plc

Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co Inc

Executive Director, Product Development Team Leader, Clinical Research, Hematology Merck & Co Inc

Associate Principal Scientist, Clinical Research Merck & Co Inc

Scientist 3 - Clinical Research Net2Source

Clinical Director, Clinical Research, Hematology Merck & Co Inc

Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co Inc

Scientist 3 - Clinical Research Artech LLC

Scientist 3 - Clinical Research eTeam Inc.

Senior Medical Science Liaison, Dermatology (Pacific Northwest) Johnson & Johnson

Senior CRA ICON Plc

Contract Senior CRA ICON Plc

Distinguished Scientist, Clinical Research, Thoracic Malignancies Merck & Co Inc

Senior Medical Director, Clinical Development - Neurodegeneration GSK plc

Senior Clinical Trial Manager ICON Plc

Senior Medical Science Liaison, Hematology - Western Michigan Johnson & Johnson

Sr. Clinical Trial Manager ICON Plc

Senior Clinical Editor ICON Plc

Senior Director, Therapeutic Area (Hepatology) ICON Plc

Research Pipeline Project Manager GSK plc

Senior Medical Director, Oncology Clinical Development - GU GSK plc

Clinical Development Scientist (Senior Director) Pfizer Inc

500320 Senior Clinical Supplies Specialist ICON Plc

Senior Manager, Clinical Project Management Olympus Corp

Senior RN Clinical Consultant, Disability Appeals The Guardian Life Insurance Company of America

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