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Commission Virtual Clinical Research Jobs (NOW HIRING)

IQVIA

Contract Virtual Clinical Coordinator

New York, NY · Remote

$33K - $82K/yr

Overview The Virtual Clinical Coordinator (temp/fixed term) plays a critical role in supporting the ... Collaborate with the research team and study sites to identify, recruit, and virtually enroll ...

IQVIA

Contract Virtual Clinical Coordinator

New York, NY · Remote

$33K - $82K/yr

Overview The Virtual Clinical Coordinator (temp/fixed term) plays a critical role in supporting the ... Collaborate with the research team and study sites to identify, recruit, and virtually enroll ...

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How much do commission virtual clinical research jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for commission virtual clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.
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What are the most commonly searched types of Virtual Clinical Research jobs? The most popular types of Virtual Clinical Research jobs are:
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Commission Virtual Clinical Research jobs near you
Infographic showing various Commission Virtual Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.
Director, Clinical Research

Director, Clinical Research

Life Extension Foundation Buyers Club Inc

Fort Lauderdale, FL • On-site

Full-time

Posted 21 days ago

Job description

General Description: Leads Life Extension Clinical Research and ensures studies are conducted in a timely, quality driven manner while following all applicable guidelines. This role is responsible for the day-to-day operations of Life Extension Clinical Research, including managing clinical studies (onsite and virtual) with a sense of urgency, within budget and with the goal of creating a Clinical Center of Excellence.

Core Duties and Responsibilities:

  • Provides overall leadership to LECR and staff by clearly communicating goals and expectations and driving productivity with a sense of urgency while ensuring 100% compliance with rules and regulations.
  • Ensure all clinical trial projects (internal and external), to include project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project timelines
  • Management and oversight of research projects and laboratory components of studies; develops appropriate study design and establishes accurate timelines; collaborates on statistical plans and data analysis
  • Prepares and/or supervises the preparation of the Protocol, Informed Consent and associated documentation for clinical studies and assures necessary project approvals from an Institutional Review Board (IRB) are obtained
  • Primary point of contact for the IRB
  • Prepares and manages all LE Clinical Research budgets
  • Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media
  • Assures all applicable regulations are implemented and followed; supervises management of data files and confidential information; follows established SOPs, i.e. for appropriate document destruction
  • Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration
  • Monitors progress of ongoing external projects that received Life Extension support and/or donated materials, assuring resupply so materials do not expire without replacement during a project
  • Supports the study team with the various tasks associated with conducting the clinical trial to ensure goals are met
  • Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance
  • Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.
  • Hires, trains and assures high quality supervision of the LE clinical research staff
  • 2 onsite days per week is an essential function of this position with flexibility to work additional onsite days as needed
  • Travels as needed
  • Additional duties as assigned

Position Requirements:

  • Bachelor’s degree in Biomedical Science, Healthcare or a Life Science related field required; Advanced degree (MSN/NP, MD, DO, PharmD, MHSA, PhD) preferred
  • 7+ years Clinical Research experience with at least 2 years in a supervisory leadership capacity preferred
  • Demonstrated leadership, ability to effectively communicate and drive positive change
  • Equally adept at running traditional in person and innovative virtual clinical studies.
  • Proactively manage LECR and readily adapt to and incorporate new technologies and platforms
  • Successfully multi-task in an entrepreneurial environment and manage multiple clinical studies in parallel