Medical Writer Jobs
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Hydrogen Group-New York
Medical Writer (On-site, 3 days/week)
We are seeking a Medical Writer to support clinical development programs through the creation of high-quality scientific and regulatory documents. This role partners closely with cross-functional teams...
Yardley
and Commercialization, Value Access and Outcomes, Medical Strategy and Communications, and Real-World Evidence.
Responsibilities / Position overview:
We are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical...
icims.com -
Hydrogen Group-New York
Job Description
Medical Writer (On-site, 3 days/week)
We are seeking a Medical Writer to support clinical development programs through the creation of high-quality scientific and regulatory documents. This role partners closely with cross...
Adecco-Morristown (NJ)
Adecco Healthcare & Life Sciences is hiring a remote part-time Medical Writer for our Pharmaceutical partner.
The anticipated hourly wage for this position is between $68 and $69.15. Hourly wage may depend upon experience, education, geographic...
adecco.com -
TalentBurst, an Inc 5000 company-Santa Clara
Medical Writer IV
Duration: 6-12 months from the start date of the worker with possibility to extend contract
Location: St. Paul, MN; Santa Clara, CA; or remote
Onsite or Remote Role-
Schedule: 8 to 5 in respective time zone; if not in PST time...
Abbott Laboratories-Abbott Park
Medical Writer II
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
• Career development with an international company...
jobs.abbott -
Meet Life Sciences-South San Francisco
Associate Director, Medical Writing
Hybrid role in South San Francisco
Individual Contributor
Key Responsibilities
• Provides medical writing leadership for clinical programs
• Acts as a medical writing subject matter expert and collaborates...
Abbott Laboratories-Maple Grove (MN)
Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process. Daily activities are related to authoring...
jobs.abbott -
Stratacuity: Proven Scientific Placement-Boston
Our Boston based pharmaceutical client is looking for a Senior Director of Medical Writing to lead the strategy, delivery, and quality of clinical and regulatory documents across their portfolio. This role partners closely with R&D teams, manages...
Costello Medical-Boston
Boston office
About the Role
The Analyst and Medical Writer positions are ideal for recent graduates in the sciences, and those with experience in scientific research, who are seeking the opportunity to apply their knowledge to real-world projects...
workable.com -
The Steely Group-Boston
The Senior Director of Medical Writing will have responsibility for executing a fit-for-purpose delivery model to produce a range of high quality clinical and regulatory documents to advance company goals across all investigational and marketed...
Remote
for new drug approval and commercialization.
Job Overview:
The Associate Principal Medical Writer (APMW)- (MedPubs Focus) will support clients by drafting medical publications with knowledge of publications processes and requirements. The APMW...
certara.com -
Exelixis-Alameda (CA)
knowledge of the theory and application of current statistical methods appropriate for data analysis and clinical trial design. Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers...
Meet Life Sciences-San Diego
of safety data, medical data trends, and emerging benefit-risk profiles
• Partner cross-functionally with Clinical Operations, Regulatory, Biometrics, Translational Sciences, Medical Writing, and other teams to support study execution
• Author and review key...
United States
collaborates with medical writer, participates in governance committee review
• Authors protocol clarification letters
• Contributor to study specific documents (e.g., SMP)
• Reviews/updates informed consent
• Provides scientific input to SM for data management...
pharmiweb.jobs -
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