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Entry Level Regulatory Medical Writer Jobs (NOW HIRING)

MJH Life Sciences

Associate Medical Writer

Cranbury, NJ · On-site

$65K - $75K/yr

Ensure compliance with ACPE and other regulatory guidelines throughout the grant development ... medical writing, scientific communications, or related role (internships considered). * Strong ...

Nucleus Global

Senior Medical Writer

Yardley, PA · On-site

Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience ...

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

Demonstrated proficiency in medical, pharmaceutical, regulatory, clinical writing * Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint, Access) * Understanding and knowledge of medical ...

ARUP

Medical Writer Editor I

Salt Lake City, UT

The Medical Writer I works with medical directors and other ARUP personnel to complete writing ... and OSHA regulations and company policies. ARUP Policies and Procedures: To conduct self in ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

Ensure high quality study documentation that is submission-ready for various regulatory agency and ... Writes and/or contributes to abstracts and submissions of clinical data to various medical ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

Ensure high quality study documentation that is submission-ready for various regulatory agency and ... Writes and/or contributes to abstracts and submissions of clinical data to various medical ...

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Entry Level Regulatory Medical Writer information

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How much do entry level regulatory medical writer jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for entry level regulatory 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 is the difference between Entry Level Regulatory Medical Writer vs Regulatory Medical Writer?

AspectEntry Level Regulatory Medical WriterRegulatory Medical Writer
Required CredentialsBachelor's degree, life sciences background, some familiarity with regulationsBachelor's or higher in life sciences, with more experience in regulatory writing
Work EnvironmentEntry-level, training-focused, often in pharmaceutical or biotech companiesMore experienced, may lead projects, work in similar settings
Employer & Industry UsagePharmaceutical, biotech, CROs, regulatory agenciesPharmaceutical, biotech, CROs, regulatory agencies

The main difference is experience level and familiarity with regulatory processes. Entry Level Regulatory Medical Writers are just starting their careers and require training, while Regulatory Medical Writers have more experience and handle complex documentation independently.

What cities are hiring for Entry Level Regulatory Medical Writer jobs? Cities with the most Entry Level Regulatory Medical Writer job openings:
What are the most commonly searched types of Regulatory Medical Writer jobs? The most popular types of Regulatory Medical Writer jobs are:
What states have the most Entry Level Regulatory Medical Writer jobs? States with the most job openings for Entry Level Regulatory Medical Writer jobs include:
Entry Level Regulatory Medical Writer jobs near you

Medical Writer - India (56829)

Praxis Precision Medicines, Inc

Boston, MA • On-site, Remote

Contractor

Re-posted 13 hours ago

Job description

Praxis is seeing a Medical Writer who will work under the guidance of the Associate Director, Medical Writing and will help support the needs of one or more clinical development programs at Praxis. You will be responsible for completing accurate, high quality, and regulatory compliant documents in support of clinical trials and regulatory submissions. This requires the knowledge and expertise to collaboratively author required documents with support and input from the Associate Director, Medical Writing while also helping other teams follow medical writing processes and style requirements. This position will be remote and located in India.
Primary Responsibilities
  • Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead on assigned documents or identifying when external writers are necessary for support
  • Supports documents for regulatory submissions to US and global health authorities, including Investigational New Drug (IND) applications, New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), protocols, investigator brochures, clinical study reports, briefing documents, regulatory responses to health authority questions, and scheduled reports.
  • Collaborates with cross-functional team members, eg, Clinical Pharmacology, Toxicology, Research, Clinical Development, Regulatory Affairs, Biostats, Data Management, Quality, CMC, QC, etc., to ensure accurate and timely completion and delivery of high-quality, scientifically-sound documents, slide decks, and publications
  • Supports clinical trial transparency and disclosures, including clinical trials registration and results posting on clinicaltrials.gov, EudraCT, and similar databases worldwide
  • Contributes to departmental development through editorial and review support for document templates, style standards, reviewer guidelines, and standard operating procedures to ensure consistent and high-quality deliverables
  • Ensures adherence to relevant SOPs and internal best practices

Qualifications and Key Success Factors
  • Bachelor's degree required within a scientific discipline. Advanced degree, CNS, and Rare Disease experience a plus.
  • A minimum of 3 years of medical writing experience in Sponsor or CRO setting
  • AMWA certification preferred
  • Experience using medical writing systems and technologies including Veeva RIM
  • Knowledge of drug development, study conduct processes, ICH guidelines, and FDA/EU guidance or demonstrated success within a regulated industry environment
  • Represents the core Praxis values of Trust, Ownership, Curiosity, and Results
  • Ability to think critically in a fast-paced environment with a keen sense of urgency and demonstrated ability in creating solutions
  • Self-motivated, able to work autonomously, and able to be a key contributor to one or more high-functioning and collaborative teams
  • Highly organized and detail-oriented with a passion to deliver quality results quickly
  • Strong verbal and written communication skills with an ability to build relationships internally and externally
  • Highest levels of professionalism, confidence, personal values, and ethical standards

Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.

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