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61 Medasource Desktop Support Analyst Jobs Hiring Near You

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

You will contribute scientifically and strategically to submission teams, plan data analyses ... Mentor and develop junior medical writers, providing guidance and support as needed * Demonstrate ...

DYOPATH

Desktop Support Analyst II

Akron, OH · On-site

$31.68/hr

Join DYOPATH as a Desktop Support Analyst II Are you passionate about solving technical challenges, supporting end users, and keeping systems running smoothly? DYOPATH is seeking a Desktop Support ...

Humetis Group

Desktop Support Analyst

Big Rapids, MI · On-site

$20 - $26.75/hr

Desktop Support Analyst Location: Big Rapids, MI 49307 Type: Contract (6+ months) Position Overview We are seeking an experienced Desktop Support Analyst to join our IT Support team in Big Rapids, MI.

Bravens

Desktop Support Analyst

White Plains, NY · On-site

$24 - $32.25/hr

Desktop Support Analyst Job Location: White Plains, NY Project Overview The Desktop Support Analyst provides handson technical support to end users across the organization, ensuring timely resolution ...

DYOPATH

Desktop Support Analyst I

Sanford, NC · On-site

$21/hr

Join DYOPATH as a Desktop Support Analyst I Are you energized by solving technical puzzles and helping people stay connected and productive? DYOPATH is looking for a Desktop Support Analyst I who ...

DYOPATH

Desktop Support Analyst I

Waco, TX

$22/hr

Join DYOPATH as a Desktop Support Analyst I Are you energized by solving technical puzzles and helping people stay connected and productive? DYOPATH is looking for a Desktop Support Analyst I who ...

Experis

Desktop Support Analyst

Lynn, MA · On-site

$25/hr

Role: Desktop support analyst Pay Rate - $25 Hourly with Benefits Location: Lynn, United States Onshore Beginner knowledge on Active Directory, Group Policy Hands on experience for Windows, & IoS ...

DCM Services

Desktop Support Analyst

Columbia, SC · On-site

$50K - $60K/yr

Description Desktop Support Analyst Full-time | Non-Exempt | Bonus Eligible About DCM Services DCM Services, LLC is a receivables management company that partners with organizations to deliver ...

Harriscomputer

Desktop Support Analyst- H

Elizabeth, NJ · On-site

$23.50 - $31.50/hr

Desktop Support Analyst Role: Desktop Support Analyst for a managed services group, providing onsite support to a major healthcare organization in New Jersey. Location: Primarily onsite in Elizabeth ...

DCM Services LLC

Desktop Support Analyst

Columbia, SC · On-site

$50K - $60K/yr

Desktop Support Analyst Full-time Non-Exempt Bonus Eligible About DCM Services DCM Services, LLC is a receivables management company that partners with organizations to deliver responsive ...

Harris

Desktop Support Analyst- H

Elizabeth, NJ · On-site

$23.50 - $31.50/hr

Desktop Support Analyst Role: Desktop Support Analyst for a managed services group, providing onsite support to a major healthcare organization in New Jersey. Location: Primarily onsite in Elizabeth ...

Harris

Desktop Support Analyst- H

Elizabeth, NJ

$23.50 - $31.50/hr

Desktop Support Analyst Role: Desktop Support Analyst for a managed services group, providing onsite support to a major healthcare organization in New Jersey. Location: Primarily onsite in Elizabeth ...

TeamSoft

Desktop Support Analyst

Cedar Rapids, IA · On-site

$20 - $28/hr

Desktop Support Analyst Location: Cedar Rapids, IA (on site 5 days/week) Pay Rate: $20/hr - $28/hr (variable dependent) Duration: 4+ months contract Description: Help Desk / Desktop Support resource ...

Altera Digital Health

Desktop Support Analyst- H

Elizabeth, NJ · On-site

$23.50 - $31.50/hr

Desktop Support Analyst Role: Desktop Support Analyst for a managed services group, providing onsite support to a major healthcare organization in New Jersey. Location: Primarily onsite in Elizabeth ...

Scalence L.L.C.

Desktop Support Analyst

Tampa, FL · On-site

$22 - $29.50/hr

They are seeking a Desktop Support Analyst to deliver exceptional customer service, provide comprehensive desktop support, and maintain accurate documentation of technical procedures.

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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.
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Infographic showing various Desktop Support Analyst job openings at Medasource in the United States as of August 2026, with employment types broken down into 20% Full Time, and 80% Contract. Highlights an 100% Physical job distribution.

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Re-posted 21 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)

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