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
- ...Principal Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity Collaborating...RegulatoryFlexible hours
$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$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$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- Criterion Edge is seeking an Associate Medical Writer to join their team in Los Angeles. The role involves supporting and leading regulatory writing projects for healthcare solutions, focusing on EU IVDR submission requirements. Ideal candidates should have experience in...RegulatoryRemote jobFull time
$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- ...A healthcare organization in Los Angeles is seeking a Regulatory Coordinator for clinical trials. The role involves managing regulatory submissions and documentation, ensuring compliance with federal and institutional guidelines. Candidates should have at least 1 year...RegulatoryHourly pay
- ...The Clinical Research Associate I works under the direction of a Clinical... ...for various clinical trials. Schedules research participants... ...supervising staff with regulatory submissions to the Institutional... ...disability, legally protected medical condition (cancer‑related or...RegulatoryDaily paidLocal area
- Direct Jobs is seeking a Regulatory Coordinator II to prepare and submit documentation to regulatory bodies such as IRB and IACUC.... ...with FDA regulations and ensuring proper documentation for clinical trials. Applicants must have a Bachelor's Degree and at least 3 years...RegulatoryRemote job
- ...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
- ...Vice President of Regulatory Affairs About the Company Pioneering medical device company developing first-in-class technologies for critical unmet clinical needs. Industry Medical Devices... ...strong understanding of clinical trial design and regulatory evidence...Regulatory
- Direct Jobs seeks a Senior Clinical Research Coordinator to oversee the operational management of clinical trials from design through closeout. You will lead multi-site activities... ...and institutions, and ensure protocol and regulatory compliance across studies. The role...Regulatory
- ...Vice President, Clinical Development About the Company Established organization... ...design and execution of clinical trials, and ensuring compliance with regulatory requirements. This role involves... ...Hiring Manager Title Chief Medical Officer Functions ~ Medical...Regulatory
- ...About This Role The Assistant Clinical Research Coordinator (ACRC) supports... .... This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and... ...clinical research principles, medical terminology, and healthcare environments...RegulatoryH1bWork at officeMonday to Friday
- ...Chief Medical Officer About the Company Clinical-stage biotechnology company developing therapies for severe... ...overseeing the execution of clinical trials and the development of new... ...trials. A deep understanding of the regulatory landscape and the ability to work...Regulatory
- ...seeking a Research Associate II based at Los Angeles Medical Center to support clinical trials focused on Cardiac Clinical Trials. This role requires... ...execution, and work onsite four days a week, ensuring adherence to GCP and regulatory requirements. #J-18808-Ljbffr...Regulatory
- ...The Position Executive Director, Regulatory Affairs will lead the Clinical Regulatory sub‑team with responsibility for US and ex‑US clinical regulatory... ...understanding of clinical regulatory requirements for trials and marketing applications (EU, UK, Canada, Australia,...RegulatoryFor contractors
- ...detail-oriented Phlebotomist to support our clinical research team. In this role, you will... ...support the success of clinical trials by ensuring timely and accurate specimen... ...in accordance with study protocols and regulatory standards. Key Responsibilities Perform...Regulatory
- ...opportunity for an experienced Clinical Research Program Manager with a... ...oncology research and academic medical centers to lead complex, high-impact clinical trial programs at the forefront of innovation... ...research operations, including regulatory compliance (FDA, IRB, GCP),...Regulatory
- ...Job Description The Clinical Research Data Associate II manages the data for assigned research... ...bioinformatics to develop and maintain trial management systems. Ensures compliance... ...skills Proven ability to adhere to regulatory requirements and ethical guidelines Licensure...RegulatoryLocal area
- ...healthcare institution in California is seeking a full-time Quantitative Study Coordinator. The role entails managing regulatory compliance for clinical trials and population-based research, requiring strong analytical skills and effective communication. Ideal candidates...RegulatoryFull time
$31.51 - $62.64 per hour
...Overview Under the direct supervision of the Clinical Trials Administrator, The Regulatory Coordinator is responsible for submitting and managing all regulatory documentation for the Institute of Urologic Oncology's clinical research portfolio according to institutional...RegulatoryHourly pay- ...Associate General Counsel, Regulatory & Technology About the Company AI-enabled precision oncology biotech firm Industry... ...cancer biology data science machine learning clinical trials drug discovery precision oncology biopharma pharma...Regulatory
- ...research department. Reporting to the Senior Clinical Administrative Director II, and working... ..., including contracts, grants, clinical trials, and philanthropic funding. Clinical... ...with financial and institutional policies. Regulatory Compliance: Collaborate with the...RegulatoryWork at office
$410k
...approximately 1.9 million patients, including clinical trials, transfusions, and other care delivery... ...multidisciplinary teams, including medical oncologists, surgeons, radiologists,... ..., and documentation in compliance with regulatory standards and institutional policies....Regulatory$36.9 - $41.03 per hour
...compliance with study protocols and regulatory requirements; and providing... ...experience. Knowledge of medical environment and terminology.... ...regulations as well as Good Clinical Practices (GCP) and HIPAA regulations... ...(EDC) systems and Clinical Trial Management Systems (CTMS). #J...RegulatoryHourly payWork experience placementLocal areaFlexible hoursAfternoon shift- ...seeking a Research Nurse II to provide hands-on treatment and monitoring for patients in clinical trials. This role involves delivering nursing care in compliance with regulatory requirements, interacting with participants, and coordinating research logistics. The ideal...Regulatory
- ...professionals are experts who provide language, regulatory, and technology solutions tailored to... ...pharmaceutical, biotechnology, and medical device companies. They help... ..., regulatory compliance, and efficient clinical trial management. Their work supports drug development...Regulatory
$280k - $320k
...position will report into Group Vice President, Regulatory Affairs. The Executive Director, Regulatory Affairs will be the leader of the Clinical Regulatory sub‑team and will have... ...clinical regulatory requirements for clinical trials and marketing applications particularly...RegulatoryFor contractors- ...at Cedars‑Sinai! The Angeles Clinic & Research Institute has established... ...certified fellowship‑trained medical oncologists, surgeons,... ...bioinformatics to develop and maintain trial management systems. Ensures... ...Proven ability to adhere to regulatory requirements and ethical...RegulatoryLocal area
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