Get new jobs by email
- ...The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related clinical documents within agreed-upon timelines. Essential Duties and...RegulatoryFull time
Ascentage Pharma
Rockville, MD5 days ago - Principal Medical Writer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer... ...quality standards are maintained. • Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as...RegulatoryContract work
- ...Regulatory Principal Medical Writer - (fully homebased) - Sponsor Dedicated Regulatory Principal Medical Writer - (fully homebased) - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success...RegulatoryContract work
- Senior/Principal Medical Writer - Regulatory - Sponsor Dedicated - CMH Experience (Home-based, US or Canada) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical...RegulatoryContract workWork from homeFlexible hours
- Regulatory Principal Medical Writer - USA - West Coast, Canada Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...RegulatoryContract workFlexible hours
- Principal/Sr Medical Writer - Publications - Sponsor Dedicated - US (Central Location) Syneos Health® is a leading fully integrated biopharmaceutical... ...head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing...RegulatoryContract workFlexible hours
- Principal Medical Writer - Full Service - Regulatory Submissions - US - Central locations Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial...RegulatoryContract workFlexible hours
- Sr Medical Writer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success... ...head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing...RegulatoryContract workFlexible hours
- ...TransCon drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We...Regulatory
- ...Overview: We are seeking a highly qualified and experienced Senior Medical Writer to join our team. The ideal candidate will have over 10 years... ...of producing high-quality, scientifically accurate, and regulatory-compliant documents. This role offers the opportunity to work...RegulatoryWork at office
- ...Job Description The Medical Writing & Disclosure Department of the GCTO organization... ...results. The Senior Informed Consent Medical Writer is responsible for developing informed... ...compliance with internal policy, regulatory requirements, and health literacy principles...RegulatoryFor contractorsWork at officeLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work3 days per week
- Sr Medical Writer, Regulatory (Home-based, US and Canada) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...RegulatoryContract workWork from homeFlexible hours
- ...Job Title: Senior Medical Writer Job Location: Virgin, UT, USA Job Location Type: Remote Job Contract Type: Contract... ...role involves crafting high-quality, scientifically accurate regulatory and clinical documents, including protocols, clinical study reports...RegulatoryContract workRemote work
- ...the immune system to attack the tumor. Position Summary: The medical writer will be responsible for the management and oversight of assigned... ...brochures, reviewing informed consent forms, and regulatory briefing materials. They will be accountable for ensuring that...Regulatory
- ...new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and... .... Furthermore, you have: Experience in authoring clinical/regulatory documents. Excellent verbal and written communication skills with...RegulatoryTemporary workFlexible hours
- We are seeking a talented and detail-oriented Medical Writer to join our team. The ideal candidate will be responsible for creating high-... ...audiences, including healthcare professionals, patients, and regulatory agencies. The Medical Writer will play a key role in developing...RegulatoryHourly payFull time
- ...development professionals specializing in medical writing, submission publishing, and... ...for our medical writing team. The medical writer will partner cross-functionally with client... ..., Clinical Operations, Biostatistics, Regulatory, and Program Management in planning and...RegulatoryRemote work
- Join to apply for the Principal Medical Writer role at Synterex . Synterex, Inc. is a global consortium of experienced clinical development... ...Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management to plan and prepare high-quality clinical...RegulatoryRemote work
- ...your passion where it meets purpose! We are looking for a Medical Policy Writer/Senior Policy Specialist who will be responsible for the development... ...mitigation + Research and incorporate customer and state regulatory requirements into Clinical Guidelines + Collaborate with...RegulatoryWork at office
- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret...RegulatoryRemote jobFull time
- The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs... ...of therapeutic areas. Opportunities to chip in to other regulatory documents may be provided. The SMW tracks their own writing projects...RegulatoryLocal area
- ...Position Summary: We are seeking a skilled and detail-oriented Medical Writer with experience in developing compliant, high-impact... ...company SOPs. Collaborate with cross-functional teams including Regulatory, Clinical, Commercial, and Legal to ensure consistency and compliance...RegulatoryContract work
- Job Summary: We are seeking a talented and detail-oriented Medical Writer to join our team. The ideal candidate will be responsible for... ...audiences, including healthcare professionals, patients, and regulatory agencies. The Medical Writer will play a key role in...RegulatoryHourly payFull time
- ...Job Title: Senior Medical Writer (Contract-to-Hire) Location: Maple Grove, MN (100% Onsite) Period: 07/28/2025 to 07/24/2026... ...required) Scope of Services The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing...RegulatoryContract workWork experience placement
- We're Hiring: Medical Writer to Pioneer the AI Era in Clinical Research PhnyX Lab is looking for a talented and experienced Medical Writer... ...that automates the drafting and search of medical and regulatory documents. We focus on solving real-world challenges in healthcare...RegulatoryHourly payContract workPart timeFreelanceRemote work
- PXL FSP is seeking to hire a Sr. Medical Writer! Job Purpose The Senior Medical Writer is responsible for the development of medical writing deliverables that support the clinical regulatory writing portfolio and works with guidance and oversight to achieve goals. Key Accountabilities...RegulatoryRemote work
- Contributes to development of global regulatory documentation strategy and execution of tactics. Conceptualizes and develops medical communications for message-driven, concise reviewer-friendly clinical documents in order to support regulatory agency review. Coordinates...RegulatoryLocal areaRemote work
- ...Job Title: Medical Writer II Location: Maple Grove, MN (100% Onsite) Rate: $40 - $45/hr Duration: 1 Year Hours: 40 Hours/Week... ...to develop, evaluate, and finalize a variety of clinical and regulatory documents. This position is fully onsite and will ensure that...RegulatoryContract work
- ...Principal Medical Writer Job at ProPharma Group in Western Springs For the past 20 years, ProPharma has improved the health and wellness... ...the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance,...RegulatoryContract work
- Connect Life Sciences is partnered with a Clinical Research organization that has multiple openings for Regulatory Medical Writers. Job Description: Under initial supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature...RegulatoryFull timeFlexible hours
