Regulatory Medical Writer: Lead Clinical Docs
Merck
Merck's Clinical and Regulatory Strategic Communications (CRSC) department creates and delivers high-quality regulated content to support our development pipeline while enabling data sharing for customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. As a Medical Writer, you will design, author, edit, and review clinical regulatory and public-facing documents, #J-18808-Ljbffr Merck
$173.2k - $272.6k
...The Director, Functional Area Geography Lead provides strategic and operational oversight... ...principles across relevant GCTO (Global Clinical Trial Operations) organizations.... ...processes that enable teams to meet critical regulatory, clinical, and operational milestones...RegulatoryFull timeContract workFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Senior Director, Functional Area Geography Lead, GDMS Clinical Data Management (CDM Country Lead) The Senior Director, Functional Area Geography... ..., and capacity-management processes; ensure local regulatory, business, and labor compliance. Ensure geography/functional...RegulatoryLocal areaRelocationVisa sponsorshipFlexible hoursShift work
$96.2k - $151.4k
...Health Literacy Medical WriterThe Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trials... ...facing materials.The Health Literacy Medical Writer, in collaboration with a project lead, develops, authors, and leads the review of accurate...RegulatoryWork at office$96.2k - $151.4k
...The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trials... ...applies knowledge and understanding of medical writing responsibilities, including... ...stakeholders while planning, authoring, and leading the documents through review and final...RegulatoryFull timeFor contractorsWork at officeLocal area- Senior Medical Writer- ICON- Remote USA ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving... ...), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity...RegulatoryRemote workFlexible hours
- ...Johnson is recruiting an Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager... ...or Allschwil, Switzerland. The role leads end-to-end validation programs for GxP systems, ensuring quality and regulatory compliance throughout SDLC. You will guide...Regulatory
$232k - $401.35k
...Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub... ...development and execution of medical and scientific strategies for... ...Clinical Team (CT). The CL leads the team to develop products... ...essential documents for global regulatory filings. The CL will manage direct...RegulatoryFull timeLocal area- Merck & Co. is seeking an experienced Clinical Imaging Scientist (Principal Scientist) to lead imaging strategy for approximately 15-25 global clinical trials... ...senior leaders to ensure high-quality execution, regulatory alignment, and timely milestones, while supporting...RegulatoryRemote job
- ...Innovative Medicine is seeking a Medical Director/Senior Medical Director-Clinical Research. The role focuses on breast... ...development program. You will lead cross-functional teams, manage study start-up, and contribute to regulatory submissions and scientific communications...Regulatory
- ...Medical WriterA Few Words About Us Integrated Resources... ...Technology (IT), Clinical Research, Rehabilitation... ...DescriptionThe Medical Writer is responsible for medical... ...therapeutic summaries, regulatory responses, internal and... ...Product Teams to prepare or lead preparation of Clinical...RegulatoryContract work
- ...States is seeking a Senior Leader for Global Clinical Trial Operations (GCTO) Program and... ...high-quality study execution. You will lead cross-functional teams across clinical operations... ...performance, risk management, and regulatory readiness in a complex global portfolio....Regulatory
- ...Merck & Co. seeks a Senior Director, Clinical Data Management TA Lead for Melanoma to oversee data management across therapeutic areas, drive portfolio strategy, and ensure quality and regulatory compliance. The role partners with TA, Geography, and Capability leads to...Regulatory
- Merck & Co. is seeking a Senior Director, Clinical Data Management Therapeutic Area Lead (Hematology) to provide strategic and operational leadership across... ..., and digital enablement across programs, ensuring regulatory compliance while #J-18808-Ljbffr Merck & Co.Regulatory
- ...Johnson is seeking an Associate Director, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team located at a... ...oversight, and maintain inspection readiness while ensuring regulatory compliance and patient safety. #J-18808-Ljbffr Johnson & JohnsonRegulatoryWork at office
$28.5 per hour
...Clinical Operations Specialist Rate: $28.50/HR Location: 770 Sumneytown Pike, West Point, PA 19486 Qualifications Education... ...pack, ship of clinical drug shipments Understand and apply regulatory/ compliance requirements relative to the role Receive,...RegulatoryWork at office- AccentCare is seeking a Director of Clinical Operations - Hospice to lead clinical teams in the Greater Philadelphia area from our King of Prussia site. The role drives quality patient care, regulatory compliance, and operational excellence while coordinating with Site...Regulatory
- ...Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research... ...analyse clinical trials, interpreting complex medical data, and contribute to the advancement... ..., ensuring accuracy and compliance with regulatory standards. Foster strong...Regulatory
- Jefferson Health in Abington, PA is seeking a Clinical Documentation Audit Specialist to perform expert CDI reviews of medical records, ensure CMS and regulatory compliance, and prepare targeted queries for physicians. You will support enterprise-wide quality initiatives...RegulatoryRemote job
- ...Johnson is seeking an Associate Director, Cross TA Clinical Risk Management to join our R&D Quality CRM team,... ...safety, and trial quality, while supporting regulatory compliance and inspection readiness. You will lead risk reviews, develop CAPA plans, and advise on quality...Regulatory
- ...Manager, Clinical OperationsICON is a global healthcare intelligence... ...Key responsibilities include:Leading and managing clinical... ...research, data management, and regulatory affairs, to ensure alignment... ...wellbeing programmes including medical, dental, and vision coverage...Regulatory
- ...specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and... ..., manuscripts, summary documents, regulatory responses, etc.). • Formally documents findings... ...also include a minimum of 3 years medical writing and DQR/QC experience of clinical...RegulatoryImmediate start
$129k - $153k
...worldwide.Position Overview: Regulatory leaders who leverage regional... ...regulatory deliverables (including leading assigned tasks) while... ...Biology, Chemistry, Pharmacology, Clinical Medicine, or related life... ...which products can address unmet medical needs and help patients lead...RegulatoryFull timeWorldwideRelocation package- Clinical Trial Liaison ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... ...clinical trials, interpreting complex medical data, and contribute to the... ...ensuring accuracy and compliance with regulatory standards. Foster strong...RegulatoryFlexible hours
- ...a Biostatistician who will provide biostatistics consulting throughout all phases of drug development, ensuring compliance with regulatory requirements. The ideal candidate will have a Ph.D. in Biostatistics or an MS with considerable experience. The role involves close...Regulatory
- ...Innovative Medicine is seeking a Principal Scientist (Manager) for Global Regulatory Affairs, CMC, to drive global regulatory strategies for large molecules, vaccines, and delivery devices. You will lead CMC submissions and align with GRA leadership across markets. The role...Regulatory
- ...Senior Corporate Governance & Compliance Lead 125-150,000 and Bonus Blue Bell, PA... ...global law firm to support Board operations, regulatory filings, and corporate governance... ...K match program up to 6%, stellar health/medical/vision benefits, paid time off, career growth...RegulatoryPermanent employmentFull timeWork at officeRelocationRelocation package3 days per week
- ## Clinical Documentation Audit SpecialistApplylocations: Montgomery County, PAtime type:... ...provides expert level CDI reviews of targeted medical records throughout the enterprise to... ...Services (CMS), Department of Health regulatory, and financial requirements. Provides an...RegulatoryDaily paidFull timeTemporary workPart timeWork at officeRemote workFlexible hoursShift work
- PSI CRO is seeking a Clinical Operations Administrative Support (COAS) to provide administrative and operational support to clinical... ...Responsibilities include exchanging information with departments/sites, maintaining tracking systems, supporting regulatory #J-18808-Ljbffr PSI CRORegulatory
$117k - $184.2k
...Early Clinical Scientist The Early Clinical Scientist coordinates the design, planning... ...thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development.... ...; clinical site training/monitoring; medical and regulatory writing Required...RegulatoryWorldwide$199k - $343.85k
...Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub... ...finding treatments and cures. We lead where medicine is going and... ...Data Management, Statistics, Regulatory, QMMC, and GMS to ensure... ...clinical studies. He/She leads the medical review of critical data...RegulatoryFull timeContract workWork experience placementImmediate start
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Medical Writer: Lead Clinical Docs. Be the first to apply!
- regulatory North Wales, PA
- clinical research regulatory North Wales, PA
- regulatory law North Wales, PA
- regulatory executive North Wales, PA
- regulatory scientist North Wales, PA
- regulatory contract North Wales, PA
- medical group North Wales, PA
- hybrid medical North Wales, PA
- non medical North Wales, PA
- medical collections work from home North Wales, PA


