NewClinical Development Medical Senior Director (MD Required) Pfizer IncClinical Development Medical Senior Director (MD Required)Collegeville, PA$274,500–$457,500 / yearProvides 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.
Clinical Development Medical Director, Oncology PfizerClinical Development Medical Director, OncologyCollegeville, PA$239,900–$399,800 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
NewSr. Finance Manager, Commercial Reporting & Analytics, Clinical Trials Division Thermo Fisher ScientificSr. Finance Manager, Commercial Reporting & Analytics, Clinical Trials DivisionAllentown, PennsylvaniaFinance Manager, Reporting & Analytics, Clinical Trials Division, is a key finance leadership role responsible for delivering actionable financial insights, scalable reporting, and analytics capabilities to support commercial and business performance. This leader will play a critical role in advancing business intelligence, automation, and analytics capabilities to support multi billion dollar revenue delivery, improve forecast accuracy, and strengthen performance management across the division.
Clinical Development Executive Medical Director, Thoracic Pfizer IncClinical Development Executive Medical Director, ThoracicCollegeville, PA$295,900–$493,100 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Clinical Development Medical Director, Hematology Pfizer IncClinical Development Medical Director, HematologyCollegeville, PA$239,900–$399,800 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Clinical Development Senior Medical Director, Breast Oncology Pfizer IncClinical Development Senior Medical Director, Breast OncologyCollegeville, PA$274,500–$457,500 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Part-Time Practical Nursing Adjunct Clinical Instructor Pennsylvania State UniversityPart-Time Practical Nursing Adjunct Clinical InstructorPAPursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). We embrace individual uniqueness, as well as a culture of belonging that supports equity initiatives, leverages the educational and institutional benefits of inclusion in society, and provides opportunities for engagement intended to help all members of the community thrive.
CRA 1, IQVIA Biotech IQVIA Holdings IncCRA 1, IQVIA BiotechCollegeville, PA$71,900–$145,300 / yearDuring these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF). You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or start‑up activities based on study needs.
FSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West Coast Thermo Fisher Scientific IncFSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West CoastAllentown, PA$85,000–$120,000 / yearAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Virology (HIV) Community MSL / Regional Medical Scientific Associate Director - West Region Merck & Co IncVirology (HIV) Community MSL / Regional Medical Scientific Associate Director - West RegionNorth Wales, PARemote$173,200–$272,600 / yearRequired Skills: Clinical Research, External Collaboration, Health Outreach, HIV Prevention, HIV Treatment, Implementation Science, Medical Affairs, Medical Virology, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Stakeholder Engagement. Communicate external stakeholder opinions, insights, and feedback on new data, clinical trends, and the evolving HIV treatment and prevention landscape to Medical Affairs HQ teams.
Virology (HIV) Community MSL / Regional Medical Scientific Associate Director - Southeast Merck & Co IncVirology (HIV) Community MSL / Regional Medical Scientific Associate Director - SoutheastNorth Wales, PARemote$173,200–$272,600 / yearRequired Skills: Clinical Research, External Collaboration, Healthcare Education, Health Outreach, HIV Prevention, HIV Treatment, Implementation Science, Medical Affairs, Medical Virology, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Stakeholder Engagement, Strategic Thinking. Communicate external stakeholder opinions, insights, and feedback on new data, clinical trends, and the evolving HIV treatment and prevention landscape to Medical Affairs HQ teams.
Mobile Application Developer Integrated Resources, IncMobile Application DeveloperCollegeville, PennsylvaniaFull timeAble to balance multiple project initiativesGeneration of appropriate documentation: project plans, requirements and design documents, use cases, storyboardsDemonstrated effective organization and time managementDemonstrated ability to deliver results under aggressive schedulesAbility to work independently and with minimum supervisionAbility to function in a dynamic work environmentDesign/develop reusable frameworks, components, and services Must have demonstrated competency / expertise in: Objective-C, Xcode, MVC and related design patternsRESTful web service (producer and consumer)Knowledge of mobile technologies and architecturesAbility to work with others in a constructive and collaborative mannerAbility to identify and resolve application defects.
Quality Compliance Associate Integrated Resources, IncQuality Compliance AssociateCollegeville, PennsylvaniaContractorThe person will be responsible for regulatory change management activities as a Site Compliance Network Member (SCNM), management of routine complaints and execution of lot disposition activities for the Drug Products and Drug Substances (APIs) manufactured by COQA managed Contractors.• Initiate, review and approve regulatory changes through the Regulatory Compliance Change Manager (RCCM) system and Product Dossier Manager (PDM) for changes initiated by or impacting COQA managed contractors.• Good command of English language• Good verbal and written communication skills and able to work in diverse multi-level, cross-divisional and multi-cultural working environment• Show strong negotiation skills and customer focus• Demonstrate ability to prioritize work, manage multiple projects act and work independently• Take initiative and proactive Some Travel (Up to 10% travel required)
NewAssociate Principal Scientist, Epidemiology Merck & Co IncAssociate Principal Scientist, EpidemiologyWest Point, PA$142,400–$224,100 / yearIn 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. Leads cross-functional interaction with risk management sub-teams, value evidence sub-teams, clinical, and regulatory sub-teams, and other R&D areas on epidemiologic matters related to product safety, risk management, post-marketing safety studies, regulatory activities, and clinical development for assigned company products.
Associate Medical Director Johnson & JohnsonAssociate Medical DirectorTitusville, NJ$137,000–$235,750 / yearRequired Skills: Preferred Skills: Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Cross-Functional Collaboration, Healthcare Trends, Leverages Information, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Scientific Communications, Strategic Thinking, Tactical Planning, Technical Credibility. The Associate Medical Director acts, in collaboration with CAPLYTA Medical Affairs leadership, to connect therapeutic strategy with the clinical, scientific, and operational implementation of U.S.-focused company-sponsored or investigator-initiated studies supporting CAPLYTA.
Medical Writer Position Integrated Resources, IncMedical Writer PositionCollegeville, PennsylvaniaContractorHighly organized, ability to prepare technical reports, summaries, protocols, and quantitative analysesTechnical Knowledge:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy. Job DescriptionResponsibilities:Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products.
Medical Writer Integrated Resources, IncMedical WriterCollegeville, PennsylvaniaContractorRESPONSIBILITIES:Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products. Additional InformationTECHNICAL KNOWLEDGE:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy.
Associate Medical Director, Rheumatology Therapeutic Area Johnson & JohnsonAssociate Medical Director, Rheumatology Therapeutic AreaHorsham, PAYou will be responsible for: Contributes to US Rheumatology Medical Affairs strategy and will actively contribute to one or more integrated evidence teams (IETs) for approved and pipeline Rheumatology products/indications, working cross-functionally with partners within the IETs, including Medical Science Liaison (MSL) team leaders, RWV&E, Field V&E, SCG, Marketing brand teams, as well as potentially Rheumatology Disease Area Stronghold (DAS), R&D, Global Medical Affairs, (MSL) and Global Commercial partners to support execution of the TA Strategy for establishing access as well as plans for evidence generation and dissemination plans. Purpose: The Associate Medical Director, Rheumatology TA, US Medical Affairs will be an important part of the Rheumatology TA team, working closely with the other Rheumatology Medical Directors (and Associate Directors) as well as partners in US and Global Medical Affairs, Real World Value and Evidence (RWV&E), Population Health, Epidemiology, R&D, Biostatistics, and US and Global Commercial Team members supporting Immunology and Rheumatology within the Johnson & Johnson organization.
Associate Director, Global Regulatory Advertising and Promotion IQVIAAssociate Director, Global Regulatory Advertising and PromotionDurham, PennsylvaniaLead discussions for assigned products during the Promotional Material Review Team (PMRT) and Medical Review Committee (MRC) working closely with Marketing, Medical, Legal, and Compliance teams to develop impactful material that aligns with regulatory expectations. The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements for promotional and non-promotional materials across various communication channels.
Associate Director, Quantitative Systems Pharmacology GSK plcAssociate Director, Quantitative Systems PharmacologyCollegeville, PA$151,500–$252,500 / yearAs an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas. This role requires a highly motivated individual to develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas.