Medasource
Medasource

45 Medasource Data Analyst Jobs Hiring Near You

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical ...

Data Analyst II * Hourly/Salary Compensation Range: 52.50/hr * Location: Remote, onsite as needed at Client Health Plan * Hours: 8:00 AM - 5:00 PM * Start Date: 7/20/26 * Client Overview: Client ...

Data Analyst II * Hourly/Salary Compensation Range: 31-37/hr (contract) * Location: Remote, onsite as needed at Client (Northern California) * Hours: 8:00 AM - 5:00 PM PST * Start Date: 7/13/2026

Data Analyst / Power BI Developer Richmond, VA Hybrid role Compensation: $40 - $45/hr Contract ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

Sr. Data Scientist

Indianapolis, IN · On-site

$80 - $88/hr

Design and execute geospatial analyses to support product and business decision-making * Build ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

Jr Data Engineer

Baltimore, MD · On-site

$30 - $40/hr

Working closely with senior engineers and analysts, you will help manage data infrastructure, build ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

GIS Analyst

Frankfort, KY · On-site

$30 - $45/hr

Perform GIS analysis, data editing, troubleshooting, and quality control * Work with customers to ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

... analytical thinking skills, particularly in troubleshooting complex data and system issues • ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

New

Systems Analyst

Pittsburgh, PA · On-site

$40 - $60/hr

Systems Analyst Pittsburgh, PA Hybrid role (Onsite and Remote) $40 - $60 per hour 12-month contract ... Ensure data quality in all supported systems and processes * Collaborate with team members, embrace ...

Lab Engineer

Centennial, CO · On-site

$30 - $40/hr

Hands-on learning across RF, signal processing, data analysis, and future AI applications * Strong mentorship and visibility through the Elevate Program Disclaimer: Brooksource, Medasource, and ...

Testing Analyst Nashville, TN (Hybrid - 2-3 days onsite) Hybrid role 12-month contract (possible ... Maintain system integrations and data flow documentation * Create training materials and knowledge ...

Analytics Project Lead

Lansing, MI · On-site

$43 - $55/hr

Coordinate across engineering, data, and platform teams to ensure alignment and successful delivery ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

Fabric or Data Lake experience a plus * Comfortable supporting analysis work under senior guidance Disclaimer: Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family ...

New

Fabric or Data Lake experience strongly preferred * Ability to lead technical analysis and present findings/recommendations independently Disclaimer: Brooksource, Medasource, and Calculated Hire are ...

New

Lead DS- Remote

Miami, FL · On-site +1

$90 - $100/hr

Lead analytical initiatives from discovery through deployment with minimal oversight. * Deliver ... data, applicable bargaining agreement (if any), or other law. Disclaimer: Brooksource, Medasource ...

Mechanical Engineer

Novi, MI · On-site

$45 - $65/hr

Whether you're hiring for software development, cloud computing, cybersecurity, data analytics, or ... Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies ...

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Medasource Jobs Information

What is it like to work at Medasource?

Medasource is a healthcare IT staffing and consulting company that values collaboration, innovation, and customer satisfaction, fostering a dynamic and supportive work environment.

The company's team structure is designed to promote open communication and knowledge sharing, with a flat organizational hierarchy that encourages employee growth and development. Medasource's mission is to deliver exceptional service and expertise to its clients, while also providing opportunities for employees to make a meaningful impact in the healthcare industry.

Working at Medasource may appeal to candidates who are passionate about healthcare technology and enjoy a fast-paced, results-driven work environment, with opportunities for professional growth and development in a company that prioritizes employee satisfaction and well-being.

What makes Medasource an attractive place to work?

Medasource is a leading provider of healthcare workforce solutions, known for its expertise in staffing and recruitment services. The company offers a dynamic work environment that values collaboration, innovation, and employee growth, with opportunities for professional development and advancement. By joining Medasource, individuals can contribute to the company's mission of delivering exceptional healthcare staffing solutions and enjoy a stable and rewarding career in a rapidly evolving industry.
What are the most popular categories at Medasource?
Infographic showing various Data Analyst job openings at Medasource in the United States as of July 2026, with employment types broken down into 2% Full Time, and 98% Contract. Highlights an 98% Physical, and 2% Remote job distribution.
Lead Medical Writer

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Posted 6 days ago


Job description

Lead Medical Writer
Remote (must be based in EST)
Compensation: $80-$90 per hour
Contract Length: 2 month Contract to Hire (40 hours/week)
Start Date: 7/1/26
ABOUT THE ROLE
Our client is a global healthcare services and products company providing pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve efficiency, reduce costs, and enhance patient care through integrated distribution and data-driven solutions. As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and responses to health authority queries. You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs. This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates must be available to work in the Eastern Standard Time zone.
WHAT YOU'LL DO
  • Autonomously write and review clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and other regulatory submissions such as responses to health authority questions, briefing books, 120-day safety updates, pediatric investigational plans, and investigator brochures
  • Contribute scientifically and strategically to submission teams at the project and/or study team level, providing input on pooling strategy, content expertise, and guidance on regulatory requirements
  • Plan and review data analyses and presentations for CSRs; review statistical analysis plans and related documents
  • Collaborate effectively with cross-functional stakeholders, including Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs
  • Work with in-house Documentation Specialists to produce high-quality final documents and ensure timely delivery
  • Mentor and develop junior medical writers, providing guidance and support as needed
  • Demonstrate advanced medical writing skills and maintain up-to-date knowledge of regulatory document requirements and guidelines
  • Work independently and as part of a team, managing multiple priorities and meeting challenging deadlines
  • Exhibit excellent interpersonal and presentation skills in all interactions
  • Maintain advanced proficiency in English for all written and verbal communications
WHAT YOU BRING
  • Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred)
  • 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas
  • Proven ability to autonomously write and review clinical regulatory documents (e.g., CTD Module II summaries, CSRs, Clinical Overviews, Investigator brochures, and other regulatory submissions)
  • Strong knowledge of regulatory document requirements and guidelines
  • Experience contributing scientifically and strategically to submission teams
  • Ability to plan data analyses and review statistical analysis plans for CSRs
  • Excellent collaboration skills with cross-functional stakeholders
  • Well-developed medical writing skills with attention to quality and deadlines
  • Ability to mentor and develop junior medical writers
  • Ability to work independently and as part of a team
  • Strong interpersonal and presentation skills
  • Advanced level of English proficiency
  • Ability to work under pressure and meet challenging deadlines
  • Remote work capability with availability in Eastern Standard Time (EST)