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Pharmacist Medical Writer Jobs (NOW HIRING)

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

We serve more than 400 pharmaceutical, biotechnology, and device organizations The Medical Writer will be responsible for the creation and development of all study start-up documents such as the Site ...

Prometrika LLC

Senior Medical Writer

Cambridge, MA · On-site

$134K - $162K/yr

Minimum of 6 years of experience in medical writing with a minimum 4 years regulatory writing in biotechnology/pharmaceutical industry SKILLS * Knowledge of ICH recommended content of Investigator ...

Celerion

Medical Writer

Compile, write and edit clinical study reports and other industry documents. Confirm accurate ... Knowledge of medical, pharmaceutical, and/or clinical research concepts preferred. Celerion Values:

Celerion

Medical Writer

OR · Remote

Compile, write and edit clinical study reports and other industry documents. Confirm accurate ... Knowledge of medical, pharmaceutical, and/or clinical research concepts preferred. Celerion Values:

Costello Medical

Analyst/Medical Writer

Boston, MA · On-site

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... pharmaceutical and device companies. Most activities have a strong patient and/or healthcare ...

Costello Medical

Analyst/Medical Writer

Boston, MA · Hybrid

$71K - $76K/yr

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical ... pharmaceutical and device companies. Most activities have a strong patient and/or healthcare ...

ProPharma Group

Senior Medical Writer

Charleston, WV · On-site

... device, and pharmaceutical organizations of all sizes to confidently advance scientific ... Strives to complete medical writing deliverables on time and within budget. * With minimal ...

Johnson & Johnson

Medical Writer III

Raritan, NJ · On-site +1

At least 6 years of relevant pharmaceutical/scientific industry experience including at least 4 years of regulatory medical writing experience! * Immunology therapeutic area experience is strongly ...

Johnson & Johnson

Medical Writer III

Titusville, NJ · On-site +1

At least 6 years of relevant pharmaceutical/scientific industry experience including at least 4 years of regulatory medical writing experience! * Immunology therapeutic area experience is strongly ...

Jj

Medical Writer III

Raritan, NJ · On-site +1

At least 6 years of relevant pharmaceutical/scientific industry experience including at least 4 years of regulatory medical writing experience! * Immunology therapeutic area experience is strongly ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Bachelor's degree in life sciences, health sciences, or a scientific field. * 5+ years of experience in medical or regulatory writing within the pharmaceutical or healthcare industry. * 3+ years of ...

CEDENT

Senior Medical Writer

Rockville, MD

D. or PharmD) Doctoral Degree+2 years of relevant corporate medical writing experience in the pharmaceutical industry, especially writing in one or more of the oncology or rare diseases therapeutic ...

Real Chemistry

Senior Medical Writer

... pharmaceutical and biotech industries. Our #LifeatRealChem culture is rooted in our people-we ... The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications ...

LanceSoft Inc

Medical Writer I

Raritan, NJ · On-site

Company Description Medical Device/ Pharmaceutical Company. The applicant will write Product Risk Assessment documents for Pharmaceutical Products and require specific experience in Risk assessments ...

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How much do pharmacist medical writer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for pharmacist medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a pharmacist medical writer?

A Pharmacist Medical Writer is typically responsible for creating, reviewing, and editing a variety of scientific and clinical documents, such as research articles, regulatory submissions, continuing education materials, or drug monographs. Daily tasks often include analyzing clinical data, collaborating with healthcare professionals or clients, and ensuring all content aligns with current guidelines and best practices. You may also participate in team meetings, manage multiple projects simultaneously, and stay updated on the latest pharmaceutical research. This role combines research, writing, and cross-functional teamwork, providing variety and the opportunity to contribute to scientific advancement.

What are the key skills and qualifications needed to thrive as a pharmacist medical writer?

To thrive as a Pharmacist Medical Writer, you need a solid background in pharmacy or life sciences, excellent written communication skills, and experience in interpreting medical literature and clinical data. Familiarity with referencing software (such as EndNote), Microsoft Office Suite, and knowledge of regulatory writing guidelines or certifications like the Medical Writing Certification (MWC) is advantageous. Attention to detail, time management, and the ability to communicate complex information clearly are crucial soft skills for this role. These competencies ensure accuracy, compliance, and the effective communication of scientific information to varied audiences.

What is a pharmacist medical writer?

A Pharmacist Medical Writer combines expertise in pharmacy and medical communication to create scientific content for healthcare professionals, regulatory agencies, and the public. They write clinical documents, drug monographs, regulatory submissions, and educational materials, ensuring accuracy and compliance with medical guidelines. This role requires strong writing skills, attention to detail, and a solid understanding of pharmacology, therapeutic guidelines, and medical research. Pharmacist Medical Writers often work in pharmaceutical companies, medical communication agencies, or as freelancers.

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What cities are hiring for Pharmacist Medical Writer jobs? Cities with the most Pharmacist Medical Writer job openings:
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Pharmacist Medical Writer jobs near you
Infographic showing various Pharmacist Medical Writer job openings in the United States as of August 2026, with employment types broken down into 55% Full Time, and 45% Contract. Highlights an 55% In-person, 9% Hybrid, and 36% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Associate Medical Writer

Bioclinica

Princeton, NJ • On-site

Full-time

Re-posted 4 days ago

Job description

Company Description
Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials. We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia. We are headquartered in Doylestown, PA. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device organizations
Job Description
The Medical Writer will be responsible for the creation and development of all study start-up documents such as the Site Manual and associated forms, as well any required Protocol Amendment Impact forms and Compliance Reports for the life of each study. The Medical Writer is also expected to provide guidance and support to the Clinical Project Management Team, including the review of Project-Specific Work Instructions and attending document-related Sponsor calls.
Primary Responsibilities
Performs study start up responsibilities by:
  • Creating, modifying and finalizing Site Manuals, associated fillable forms, Quick Reference Guides and labels
  • Creating, modifying and finalizing Image Quality Assessment/Photograph Quality Assessment (IQA/PQA) Summaries
  • Creating, modifying and finalizing Quality Control (QC) Summaries
  • Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Notes to File (NTFs), Corrections and Deviation Reports
  • Creating, modifying, and finalizing Key Points Documents (KPDs) from CRs
  • Creating, modifying and finalizing paper Source Documents based on ToOs
  • Creating, reviewing, modifying and finalizing MedComm Meeting Minutes
  • Attending internal and external meetings relating to the Site Manuals, IQA/PQA/QC Summaries, CRs/KPDs, Source Documents and any other MedComm-related study start-up documents
  • Running Scheduled Tasks for generating MedComm webpages
  • Maintaining MedComm document webpages
  • Checking MedComm webpages for errors
  • Performing Project Close-outs as they occur based on receipt of Study Closure forms
  • Reviewing and updating Charter Training Slides (CTS) and CTS quiz(zes) as needed
  • Documenting study-specific Protocol Training (Kick-off Meeting Slides, Protocol Overview Presentations, etc.) by filling out and collecting signatures on group training forms as required

Manages the clinical study document development process by:
  • Creating, modifying, finalizing and attaching signed final Compliance Reports (CRs) to Final MedComm documents or review Project Team-created CRs
  • Updating the MedComm database every time a document is created, sent out for internal or Sponsor review, finalized, deemed inactive/on-hold, or cancelled
  • Providing guidance to assigned Project Teams and Project Team members
  • Providing language updates, as required, for all MedComm document templates as needed
  • Creating Final Effective documents

Secondary Responsibilities
Maintains Quality Service and Departmental Standards by:
  • Reading, understanding and adhering to organizational Standard Operating Procedures ("SOP")
  • Updating department SOPs and Work Instructions as needed
  • Assisting in establishing and enforcing departmental standards

Contributes to team effort by:
  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Participate in internal training activities
  • Helping others to achieve results
  • Performing other duties as assigned

Maintains Technical and Industry Knowledge by:
  • Staying up-to-date on response criteria publications posted by Medical Communications
  • Participating in Medical Writing Training activities, including creating/reviewing training modules
  • Participating in Clinical Project Management Training activities, including creating/reviewing training modules
  • Attending and participating in applicable company-sponsored training

Qualifications
Education:
  • Bachelor's Degree in either the Life or Physical Sciences (e.g., Biology, Chemistry, Physics, Pharmaceutics, etc.) preferred

Experience:
  • 1+ years medical writing experience required
  • 2+ years of experience in pharmaceutical/clinical/imaging research preferred
  • Demonstrated proficiency in medical, pharmaceutical, regulatory, clinical writing
  • Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint, Access)
  • Understanding and knowledge of medical and/or clinical trial terminology desired

Additional skill set:
  • Ability to work in a group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Organization and time management skills for managing multiple projects concurrently

Additional Information
Working conditions:
  • Travel: 0-5%
  • Lifting: 0-10lbs
  • Other: Computer work for long periods of time

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

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