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
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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$110.1k - $220.1k
...Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere... ...Medical Writer , you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices....RegulatoryFull timeTemporary workRemote workFlexible hours$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$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- ...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
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$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- Cedars-Sinai seeks a Clinical Research Coordinator I to independently coordinate studies in the Surgery Chair Department. You will screen... ...documentation, and support sponsor queries while maintaining regulatory compliance. You will work with FDA/IRB processes, monitor...Regulatory
$28 - $30 per hour
Kelly Science & Clinical is seeking a Clinical Research Coordinator for a 5-month temporary position at a clinical research company in... ..., screen and enroll participants, manage data, and ensure regulatory compliance while supporting investigators. Schedule is Monday-...RegulatoryTemporary workMonday to Friday- ...and procedures to ensure compliance with regulatory agencies. Assists with entry-level... ...analysis to support research project or clinical trial.Hourly salary range: 33.09 - 65.77QualificationsBasic... ....Basic knowledge of statistical and/or medical terminology.Basic ability to summarize...RegulatoryHourly payWork at office
- ...Profit Founded 1898 Employees 1001-5000 Categories Clinical Trials Health Care Hospital Medicine Specialties... ...for providing legal support in other areas as needed, such as regulatory guidance and contract interpretation, and will interface with...RegulatoryContract workWork at office
- ...Cancer Research in Los Angeles, CA is hiring a Clinical Research Coordinator to support early phase oncology trials under supervision. You will ensure accurate conduct... ...patient participation, and help maintain regulatory compliance with GCP. Strong attention to detail...Regulatory
$26.77 - $34.32 per hour
...University of Southern California (USC) in Glendale, CA, is seeking a Clinical Trials Data Manager to read and extract data from medical records and enter it into eCRFs/CRFs while ensuring regulatory compliance. You will interact with sponsors, QA teams, and monitor visits...RegulatoryHourly pay- ...an Assistant Statistician to assist with documentation and procedures ensuring regulatory compliance and to provide entry-level statistical analysis for research projects or clinical trials. The role supports ongoing studies, with an hourly salary range and a schedule...RegulatoryHourly pay
- Arrowhead Pharmaceuticals, Inc. in Pasadena, CA is seeking a Clinical Quality Assurance Specialist to support GCP compliance and QA activities... ...assist in GCP quality event management, risk-based audits, regulatory inspections, CAPAs, and collaboration with Clinical Operations...Regulatory
- Kelly Services is seeking a Clinical Research Coordinator for a 5-month temporary position at a clinical research company in West Hills, CA. This role supports study visits, data management, and regulatory compliance to deliver high-quality research outcomes. Responsibilities...RegulatoryTemporary work
- UCLA Outpatient Clinics is seeking an entry-level statistician to assist in developing documentation and procedures ensuring regulatory compliance. You will support entry-level statistical analyses... ...for research projects or clinical trials and help construct clear tables and...Regulatory
- Adventist Health Glendale is seeking a Clinical Research Coordinator to coordinate and participate in clinical studies under the guidance of principal investigators, ensuring data integrity and regulatory compliance. You will manage data collection from patient charts and...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- Cedars-Sinai in Beverly Hills is seeking a Research Nurse Coordinator III to oversee clinical study coordination, participant enrollment, data integrity and regulatory compliance within a hybrid setting. The role requires onsite four days per week in the Los Angeles area...Regulatory
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- ...an entry-level support analyst to assist with documentation and procedures for regulatory compliance and to perform entry-level statistical analysis for research projects or clinical trials. Responsibilities include creating tables/graphs, learning statistical techniques...Regulatory
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- ...About this Role: The Assistant Clinical Research Coordinator (ACRC)... .... This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional... ...clinical research principles, medical terminology, and healthcare...RegulatoryH1bWork at officeMonday to Friday
- UCLA Outpatient Clinics in Los Angeles seeks a Clinical Research Supervisor to provide immediate supervision of routine research study... ...and oversee unit operations for compliance with policies and regulatory standards. You will supervise all phases from design through...RegulatoryImmediate start
$120k - $175k
...culture that maintains compliance with all regulatory requirements at all times Create an... ...equivalent Experience with Electronic Medical Records a must An experienced leader, who... ...conduct some of the world’s leading clinical trials for cancer treatment right here in our...RegulatoryFull timeTemporary workWork at officeLocal areaWorldwideFlexible hours
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