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Associate Weekend Clinical Research Jobs (NOW HIRING)

Mayo Clinic

Clinical Research Coordinator

Rochester, MN · On-site

$27.99 - $41.98/hr

Associate's in Clinical Research from an accredited academic institution without experience OR ... Weekend Schedule Typically, Monday - Friday, with the possibility of weekends, depending on the ...

Charter Research

Clinical Research Liaison

The Villages, FL

$20.75 - $27.75/hr

Associate's degree required, Bachelor's degree preferred. Experience * Clinical research or patient recruiting experience strongly preferred. * Knowledge of medical terminology preferred. PHYSICAL ...

Wake Research

Clinical Research Site Manager

Raleigh, NC · On-site

Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) or equivalent certification, preferred. * 5+ years of relevant experience as a clinical research associate ...

Wake Research

Clinical Research Site Manager

Raleigh, NC · On-site

Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) or equivalent certification, preferred. * 5+ years of relevant experience as a clinical research associate ...

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How much do associate weekend clinical research jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for associate weekend clinical research in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.
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Associate Weekend Clinical Research jobs near you

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted 12 hours ago

Job description

Job Title: Clinical Research Associate/Monitor
6 months contract to perm
Work location: REMOTE
Required 30%-50% traveling
Candidate home location: required within DC, VA, MD only (a candidate needs to reside in DC, VA, MD)
Multiple Regional CRAs: 5 openings
USC/GC required
Search Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA III, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, Phase I, Study Monitor, Contract Monitor, CRA, Research Associate
Multiple Studies with Health patients - Previous Phase I experience required
Contract CRAs, regional based with strong monitoring skills, minimum 3-5+ years monitoring experience within the pharmaceutical industry required traveling of minimum of 50% traveling to 1-2 sites within the same state as required. Require 100% commitment and contractors paid hourly. Therapeutic areas can range and candidates will be expected on working on about 6-8 protocols (max at 10 protocols) with different indications. Multiple sites and candidate has to be local to DC, VA, and MD areas.
Minimum 3-5+ years of CRA / Monitoring experience required
Start date is ASAP
TRAVEL INFORMATION FOR CANDIDATES -
The client is working to ensure candidates are as close as possible to their sites. Company is constantly adding new studies to the monitoring project. Monitors may be asked to take on additional sites closer to their home (or maybe a bit further then what they currently have) - they will work to keep travel as regionally located as possible. There are multiple sites in each region (depends on the allocation of the individual CRAs)
In addition they should be very clear about their monitoring experience showing that they are a Regional CRA/monitor currently. (I would say 3 years monitoring experience with Oncology study required) Candidates need to allocate 50% to 100% of their time to this assignment, preferred candidates home is close to the site locations (listed above).The CRA/Study Monitor designated activities include site visits, trial monitoring, tracking, documentation, collection, solicitation and review of (e) CRFs and submit data, preparation of reports, regulatory review and participation in teleconferences. Approximately 50% travel will be required, as the CRA Study Monitor's primary responsibilities will be monitoring of study sites.
Requirements
A strong healthcare background with at least 1-2 years prior monitoring Oncology study experience is required. Phase I research experience as a monitor, auditor, research coordinator, research associate or similar oncology research experience is required. The CRA/Study Monitor must hold a Bachelor's degree from an accredited college or University or be a grad from an accredited school of nursing.
Requirement:
  • 2+ years prior monitoring Oncology study experience is required. preferred. Phase I-IV research experience as a monitor, clinical research associate experience is required.
  • BS/BA in life sciences or health-related discipline, BSN, Bachelor of Science - Nursing, Pharmacy is highly desirable.
  • Minimum 3-5+ years clinical research monitoring experience including years in Phase I studies.
  • Strong working knowledge of GCPs, ICH Guidelines, and FDA Regulations
  • Ability and willingness to travel up to 50 % of the time, including minimum overnight stays travel as necessary
  • Experience with regulatory document review/collection and IRB submissions (including OHRP regulations), a plus
  • Experience with using a Trial Master File, a plus.

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