Medical Writer: Clinical Trials and Regulatory Docs
R & D Partners
R&D Partners is looking for a Medical Writer in Los Angeles, CA. This role involves supporting the development of clinical trial materials, conducting literature reviews, and collaborating with cross-functional teams to ensure compliance with medical research standards. The ideal candidate will have 2-4 years of relevant experience and a Bachelor's degree in life sciences or healthcare. Benefits include medical, dental, vision insurance, a 401k plan, and more. #J-18808-Ljbffr R&D Partners
- YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. You will author and review CSRs...RegulatoryRemote job
$145k - $155k
Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory teams to produce a range of medical documents for regulatory submissions, including clinical evaluation reports and study protocols...RegulatoryRemote job- MiniMed is seeking a Technical Writer to draft and revise patient-facing literature for a broad medical device portfolio. You will work with subject matter experts to ensure content accuracy and compliance, and collaborate with design teams on visuals and branding. The...Suggested
$145k - $155k
Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote) Position Overview This is a Temp-To-Hire Position Primary contact... ...Some typical job duties include: Collaborating with the clinical & regulatory teams to write clinical documents for regulatory submissions...RegulatoryRemote jobTemporary workInterim role- Senior Medical Writer - Pharmaceutical & Regulatory Immix Biopharma, Inc. Our 3 Core Values Integrity Initiative... ...will play a critical role in the clinical development department, responsible... ...through various stages of clinical trials. Draft, review, and finalize regulatory...RegulatoryOdd job
- Immix Biopharma, Inc. seeks a Senior Medical Writer to prepare, review, and edit regulatory documents for FDA submissions, ensuring accuracy and regulatory compliance... ..., NDA, and BLA programs. You will collaborate with clinical, regulatory, and scientific teams, manage multiple...Regulatory
$60k - $65.58k
Medical Writer job at R&D Partners. Los Angeles, CA. Job Description R&D Partners is seeking... ...the development and submission of clinical trial education materials to the Promotional... ...functional teams including Medical Affairs, Regulatory and Marketing to ensure that materials...Regulatory$50 - $80 per hour
...Description Job Description Job Title: Medical Writer Expert Remote Location: Remote Job Type... ...seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy...RegulatoryRemote jobFor contractors- ...compliance with state, federal, and institutional regulatory requirements (e.g., Food and Drug Administration (... ...for internally funded standard projects.Conducts clinical research by: collecting data in clinical trials (e.g., recruiting human subjects, administering surveys...RegulatoryFor contractorsFor subcontractorLocal area
$27.32 - $34.67 per hour
...Must be comfortable with computers and medical terminology. In-depth knowledge of all... ...including government health programs, regulatory requirements, ability to calculate patient... ...-to-the-minute research and innovative clinical trials. The hourly rate range for this...RegulatoryHourly payFull timeWork experience placementLocal areaShift workWeekend work- ...Direct Jobs is seeking a Senior Clinical Research Coordinator to support the operational management of clinical research activities... ...for Pelvic Health and Wellness. The role includes coordination, regulatory compliance, IRB submissions, budgeting, and data management to...Regulatory
- ...Practitioner/Physician Assistant (Sub-Investigator) to maintain trial quality and regulatory compliance. You will perform study visits, collect data,... .... Requires Master’s degree and NP/PA license; 2+ years clinical research preferred, with phlebotomy and IV/infusion...Regulatory
$25 - $33 per hour
...industry’s most progressive and diversified clinical trial organizations, with strong capabilities... ...the day Request and manage medical records and related documentation Communicate... ..., and maintain organized clinical and regulatory files Manage invoices, receipts, and...RegulatoryHourly payWork at officeLocal areaMonday to FridayDay shift$49.4k - $73.5k
...seeking a Mortgage Loan Processor in Los Angeles to manage loan documentation from submission to underwriting, ensuring accuracy and regulatory compliance. You will work with borrowers and Mortgage Loan Officers to gather required documents and track processing status. The...Regulatory$65 per hour
...Clinical Research Coordinator Hourly pay: $65/hr Worksite: Leading medical institution (Los Angeles, CA 90024 - Onsite) W2 Employment... ...sponsor, institutional, and regulatory requirements. This role... ...diverse portfolio of clinical trials. Responsibilities:...RegulatoryHourly payShift work$22 - $30 per hour
Medix™ is seeking a Clinical Research Assistant in Los Angeles, CA to support the planning and execution of clinical research studies... ...recruitment while adhering to Good Clinical Practice (GCP) and regulatory requirements. The ideal candidate will have an associate...RegulatoryHourly pay- Thecardiacsuite is seeking a Clinical Research Associate to support clinical research protocols and assist in maintaining regulatory compliance. This position involves collaboration... ...adherence to regulations during clinical trials. The ideal candidate will have at least...Regulatory
- Cedars-Sinai is hiring a Clinical Research Associate I to support noncomplex studies under supervision. You will assist with data collection, scheduling, and regulatory activities while ensuring compliance with HIPAA and federal guidelines. The role emphasizes proactive...Regulatory
- ...leading healthcare institution in Los Angeles seeks a Senior Regulatory Coordinator to prepare and submit protocols to regulatory bodies... ...candidate will have a Bachelor's Degree and three years of clinical research experience, preferably with knowledge of regulatory affairs...Regulatory
- Ampcus Inc. is seeking a Senior Clinical Research Coordinator in Los Angeles, CA to oversee day-to-day conduct of clinical trials, ensuring sponsor, institutional, and regulatory compliance. This role provides leadership and mentorship to research staff and supports execution...Regulatory
- University of California - Los Angeles Health seeks a Clinical Research Center Supervisor to oversee research study coordination and ensure compliance with regulatory standards. The role requires managing clinical trial activities effectively while liaising with various...Regulatory
- Merck & Co. is seeking a Clinical Research Site Manager to oversee performance and regulatory compliance for assigned sites in the United States. The role acts as the primary site contact, ensures study conduct adheres to ICH/GCP guidelines, and drives site readiness and...RegulatoryRemote work
- Cedars-Sinai seeks a Regulatory Coordinator II to manage regulatory submissions for pre- and post... ...team, monitors, sponsors, and staff, maintain trial files, and help improve SOPs. A nursing/health science background with clinical research experience is required. #J-18808-...Regulatory
- ...The Clinical Research Associate I works under the direction of a Clinical Research Coordinator... ...participants for various clinical trials. Schedules research participants for research... ...only. Assists supervising staff with regulatory submissions to the Institutional Review...RegulatoryDaily paidFull timeLocal area
- Elite Clinical Network in Northridge, California, is seeking a highly organized Clinical Research Coordinator... ...will coordinate and support all aspects of clinical trials, including recruitment, data collection, regulatory compliance, and specimen handling. Candidates with...Regulatory
- Abbott is seeking a Senior Clinical Project Manager to lead complex clinical studies, ensuring regulatory alignment and strategic delivery across R&D, Regulatory Affairs... ...Sylmar, CA, this on‑site role requires strong medical device knowledge and ISO regulatory...Regulatory
- Cedars-Sinai Medical Center in Los Angeles is looking for a Clinical Research Associate I to manage and implement clinical research studies. You will evaluate research data, assist with regulatory submissions, and coordinate patient visits. An ideal candidate has a Bachelor...RegulatoryLocal area
- DescriptionJob Summary: Collects data for clinical trials research, independently. Prepares and/or supports the submission of study documentation to regulatory bodies (e.g., IRB) for pre-implementation review and approval. May support clinical trials activities and research...RegulatoryFor contractorsFor subcontractorLocal area
$85k - $130k
...align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a...RegulatoryWork at officeRemote work2 days per week- Exer Urgent Care in Sherman Oaks, CA is seeking a Clinical Research Coordinator II to manage the full study lifecycle with autonomy, from feasibility to data collection and regulatory compliance. The role requires coordinating patient recruitment, conducting visits, and...Regulatory
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