ZipRecruiter

Log In

1

Contract Medical Documentation Jobs (NOW HIRING)

Revolution Medicines

Principal Medical Writer

Mentors junior and contract medical writers on both document and timeline management. Required Skills, Experience and Education: * 8-11 years of clinical regulatory writing experience within one or ...

TalentBurst, Inc

Local Contract CMA

Berwyn, PA · On-site

$16.25 - $21/hr

Local Contract Medical Assistant - Abramson Cancer Center (Valley Forge) Duration: 13 Weeks ... Obtain and document vital signs. * Perform EKGs. * Room patients and prepare them for provider ...

BMT CONSULTING INC

Be Seen First

ON-CALL MEDICAL COURIER DRIVER- NEEDED ASAP

Hampton, VA · On-site

$17 - $19/hr

Hiring for open positions is contingent upon the award of the contract. Medical Driver (5 days M-F ... Deliver Hazardous material and confidential documents * Must have a "Clean" DMV report for the last ...

paradigm

Provider Contract Lead

Tampa, FL · On-site

$84K - $112K/yr

Develops and implements provider network and contract strategies, identifying the ambulatory ... and/or providing medical documentation in a timely manner. * Perform additional duties as ...

paradigm

Provider Contract Lead

Tampa, FL

$84K - $112K/yr

Develops and implements provider network and contract strategies, identifying the ambulatory ... and/or providing medical documentation in a timely manner. * Perform additional duties as ...

previous pagenext page

Showing results 21-40

All Jobsfreelance JobsHealthcare JobsContract Medical Documentation Jobs

Contract Medical Documentation information

See salary details

$20

$35

$54

How much do contract medical documentation jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for contract medical documentation in the United States is $35.98, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $50.00 per hour, depending on experience, location, and employer.

What is the difference between Contract Medical Documentation vs Contract Medical Coding?

AspectContract Medical DocumentationContract Medical Coding
Primary RolePreparing detailed medical reports and documentation based on patient recordsAssigning standardized codes to diagnoses and procedures for billing and record-keeping
Required CertificationsMedical degrees, certifications in medical documentation or health information managementCertified Professional Coder (CPC), Certified Coding Specialist (CCS)
Work EnvironmentHospitals, clinics, healthcare facilities, remote optionsHospitals, billing companies, insurance firms, remote options
Industry UsageHealthcare providers, legal cases, insurance claimsMedical billing, insurance reimbursement, healthcare compliance

In summary, Contract Medical Documentation focuses on creating detailed medical reports and records, while Contract Medical Coding involves translating medical information into standardized codes for billing and administrative purposes. Both roles are essential in healthcare but serve different functions within the medical documentation and billing process.

What cities are hiring for Contract Medical Documentation jobs?

Cities with the most Contract Medical Documentation job openings:

What are the most commonly searched types of Medical Documentation jobs?

The most popular types of Medical Documentation jobs are:

What states have the most Contract Medical Documentation jobs?

States with the most job openings for Contract Medical Documentation jobs include:

Contract Medical Documentation jobs near you

Principal Medical Writer

Revolution Medicines

Remote

Full-time

Posted 25 days ago

Job description

The Opportunity:
Revolution Medicines is seeking a motivated individual with a clinical regulatory writing background to play a critical role in the successful preparation of high-quality, submission-ready clinical research documents. This role is an individual contributor with team leadership responsibilities, reporting to the Executive Director, Medical Writing.

This position is responsible for drafting and managing the content and reviews of clinical regulatory documents for Revolution Medicines products in various drug development phases.

  • Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs, CSRs, briefing documents, periodic safety reports, risk management documents, and IND and NDA modules.

  • Assists in developing and maintaining document templates, department standard processes and work instructions, medical writer onboarding materials, and style guide.

  • Serves as primary medical writing contact for one or more clinical development programs.

  • Represents medical writing at cross-functional planning meetings.

  • Effectively communicates deliverables needed, the writing process, and timelines to team members.

  • Schedules document reviews and manage adjudication meetings.

  • Holds team members accountable to agreed-upon project dates.

  • Independently resolves document content issues and questions.

  • Ensure consistency, clarity, and accuracy both within and across documents.

  • Recognizes potential scheduling and resource conflicts across projects and provides recommendations to resolve.

  • Mentors junior and contract medical writers on both document and timeline management.

Required Skills, Experience and Education:

  • 8-11 years of clinical regulatory writing experience within one or more biopharmaceutical companies, including prior experience working as a medical writer for a BLA/NDA/MAA.

  • Advanced degree in clinical or life sciences, English, journalism, and/or communications.

  • Proficiency in Microsoft Word, including the use of MS Word styles and templates.

  • Familiarity with AMA style.

  • Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.

  • Ability to work in a high-pressure environment with short deadlines while remaining calm, focused, professional, diplomatic, and positive.

Preferred Skills:

  • Experience with oncology therapeutics.

  • Familiarity with StartingPoint, EndNote, Veeva RIM, and Smartsheet.

  • Experience performing QC reviews of clinical regulatory documents. 

    #LI-Hybrid #LI-JC1

Apply