The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Medical, dental, and vision insurance FSA, HSA Voluntary Critical Illness, Hospital Indemnity, and ...
The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Medical, dental, and vision insurance FSA, HSA Voluntary Critical Illness, Hospital Indemnity, and ...
Clinical Research Associate - Clinical Research Coordinator Experience
Cincinnati, OH · Remote
$23.25 - $31/hr
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including ... Assess the clinical research site's patient recruitment and retention success and offering ...
Clinical Research Associate - Clinical Research Coordinator Experience
Cincinnati, OH · Remote
$23.25 - $31/hr
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including ... Assess the clinical research site's patient recruitment and retention success and offering ...
Clinical Research Coordinator
Boston, MA · On-site
$60K/yr
Job Type Full-time Description An exciting opportunity for a Clinical Research Project Coordinator ... Voluntary Insurance: life, critical illness, hospital indemnity, accident, * Voluntary Benefits ...
Clinical Research Coordinator
Boston, MA · On-site
$60K/yr
Job Type Full-time Description An exciting opportunity for a Clinical Research Project Coordinator ... Voluntary Insurance: life, critical illness, hospital indemnity, accident, * Voluntary Benefits ...
Clinical Research Coordinator
Kenmore, NY · On-site
$26 - $30/hr
Clinical Research Coordinator Location: Buffalo, NY Type: Contract Compensation: $26.00 - $30.00/hr ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Clinical Research Coordinator
Kenmore, NY · On-site
$26 - $30/hr
Clinical Research Coordinator Location: Buffalo, NY Type: Contract Compensation: $26.00 - $30.00/hr ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Clinical Research Nurse
Lubbock, TX · On-site
$60K - $145K/yr
... volunteers, students, new employees. * Attend affiliated clinical research meetings and professional meetings where research and compliance training may occur. * Obtain SoCRA (CCRP) or ACRP (CCRC ...
Clinical Research Nurse
Lubbock, TX · On-site
$60K - $145K/yr
... volunteers, students, new employees. * Attend affiliated clinical research meetings and professional meetings where research and compliance training may occur. * Obtain SoCRA (CCRP) or ACRP (CCRC ...
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Experienced Clinical Research Coordinator
Pasadena, CA · On-site
$26.50 - $35.25/hr
Supervise research staff and volunteers, providing guidance on clinical research methods and compliance management Skills * Proven supervising experience in a clinical or research setting with strong ...
Quick apply
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Experienced Clinical Research Coordinator
Pasadena, CA · On-site
$26.50 - $35.25/hr
Supervise research staff and volunteers, providing guidance on clinical research methods and compliance management Skills * Proven supervising experience in a clinical or research setting with strong ...
Clinical Research Coordinator
Kenmore, NY · On-site
$26 - $30/hr
Clinical Research Coordinator Location: Buffalo, NY Type: Contract Compensation: $26.00 - $30.00/hr ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Quick apply
Clinical Research Coordinator
Kenmore, NY · On-site
$26 - $30/hr
Clinical Research Coordinator Location: Buffalo, NY Type: Contract Compensation: $26.00 - $30.00/hr ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Quick apply
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Clinical Research Coordinator- Manhattan, NY
New York, NY · On-site
$66K - $75K/yr
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1#LI-ONSITE Employment Type: Full-Time
Clinical Research Coordinator- Manhattan, NY
New York, NY · On-site
$66K - $75K/yr
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1#LI-ONSITE Employment Type: Full-Time
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Less travel hours may apply for projects with remote/virtual visits. * Must maintain a valid driver ...
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Less travel hours may apply for projects with remote/virtual visits. * Must maintain a valid driver ...
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Clinical Research Coordinator- Manhattan, NY
New York, NY · On-site
$66K - $75K/yr
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Clinical Research Coordinator- Manhattan, NY
New York, NY · On-site
$66K - $75K/yr
Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options. The IMA Group is an ... virtual capabilities. #LI-BC1 #LI-ONSITE
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Less travel hours may apply for projects with remote/virtual visits. * Must maintain a valid driver ...
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Less travel hours may apply for projects with remote/virtual visits. * Must maintain a valid driver ...
Clinical Research Coordinator
New Port Richey, FL · On-site
$26 - $30/hr
Clinical Research Coordinator Location: New Port Richey, FL - 100% onsite Type: 4 month Contract ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Quick apply
Clinical Research Coordinator
New Port Richey, FL · On-site
$26 - $30/hr
Clinical Research Coordinator Location: New Port Richey, FL - 100% onsite Type: 4 month Contract ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Clinical Research Coordinator I/II
$30 - $44.69/hr
Voluntary benefits About Us The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities ...
Clinical Research Coordinator I/II
$30 - $44.69/hr
Voluntary benefits About Us The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities ...
Clinical Research Coordinator I/II
$30 - $44.69/hr
Voluntary benefits The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to ...
Clinical Research Coordinator I/II
$30 - $44.69/hr
Voluntary benefits The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to ...
Clinical Research Coordinator
New Port Richey, FL · On-site
$26 - $30/hr
Clinical Research Coordinator Location: New Port Richey, FL - 100% onsite Type: 4 month Contract ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
Clinical Research Coordinator
New Port Richey, FL · On-site
$26 - $30/hr
Clinical Research Coordinator Location: New Port Richey, FL - 100% onsite Type: 4 month Contract ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting ... Ensures accurate data collection, documentation organization, and safety of study volunteers.
At Houston Methodist, the Clinical Research Specialist position is responsible for supporting ... Ensures accurate data collection, documentation organization, and safety of study volunteers.
Clinical Research Nurse
Pensacola, FL · On-site
$70K/yr
Clinical Research Nurse The Clinical Research Nurse will be responsible for responding to patient ... and volunteers; maintain contact with public agencies which are involved with aspects of the ...
New
Clinical Research Nurse
Pensacola, FL · On-site
$70K/yr
Clinical Research Nurse The Clinical Research Nurse will be responsible for responding to patient ... and volunteers; maintain contact with public agencies which are involved with aspects of the ...
New
Clinical Research Coordinator I/II
Seattle, WA · On-site
$25.66 - $37.21/hr
Voluntary benefits About Us The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities ...
Clinical Research Coordinator I/II
Seattle, WA · On-site
$25.66 - $37.21/hr
Voluntary benefits About Us The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities ...
Voluntary Virtual Clinical Research information
See salary details
$13.22 - $15.73
11% of jobs
$15.73 - $18.25
10% of jobs
$19.41 is the 25th percentile. Wages below this are outliers.
$18.25 - $20.76
7% of jobs
$20.76 - $23.27
19% of jobs
The median wage is $23.45 / hr.
$23.27 - $25.79
37% of jobs
$25.79 - $28.30
0% of jobs
$28.30 - $30.81
3% of jobs
$30.81 - $33.33
3% of jobs
$33.33 - $35.84
3% of jobs
$35.84 - $38.35
3% of jobs
$38.35 - $40.87
3% of jobs
$13
$24
$40
How much do voluntary virtual clinical research jobs pay per hour?
What is the difference between Voluntary Virtual Clinical Research vs Clinical Research Coordinator?
| Aspect | Voluntary Virtual Clinical Research | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires knowledge of clinical trial processes, basic healthcare or research background | Requires clinical research certifications (e.g., CCRP), healthcare background often preferred |
| Work Environment | Remote, virtual setting often involving online data collection and participant communication | On-site or hybrid settings at research sites or hospitals |
| Employer & Industry | Pharmaceutical companies, research organizations, biotech firms | Hospitals, research institutions, pharmaceutical companies |
| Search & Comparison | Often searched together due to overlapping clinical trial roles | Commonly compared as a hands-on role in clinical trials |
In summary, Voluntary Virtual Clinical Research involves remote, online-based activities, while Clinical Research Coordinators typically work on-site managing trial logistics. Both roles support clinical trials but differ mainly in work environment and specific responsibilities.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 17 days ago
Job description
Role Objectives:
The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs. They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready. The Senior CRA builds strong relationships with sponsors and sites, serving as a key point of contact throughout the study. They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.
Complex Study Experience Required
The Ideal Candidate:
- Leader
- Detail Oriented
- Problem Solver
- Adaptable
What You'll Do:
- Contribute to the design and review of study documents (protocols, CRFs, ICFs, and study plans).
- Lead site feasibility activities: distribute/collect questionnaires, evaluate responses, conduct SQVs, and recommend sites for selection.
- Planned and conducted SIVs, routine monitoring, and close-out visits in line with protocol, ICH-GCP, and regulatory requirements.
- Build strong relationships with site staff; deliver training and ongoing guidance on protocol compliance and regulations.
- Verify source data and CRFs for completeness, accuracy, and consistency; always keep site files audit-ready.
- Review IP accountability, safety event documentation, and protocol deviations; drive corrective and preventative actions.
- Manage and resolve data queries, analyze error trends, and provide targeted retraining to prevent recurrence.
- Track and close action items within study or company timelines; maintain clear oversight of monitoring deliverables.
- Support investigator meetings and key internal/external meetings; contribute to SOPs, monitoring tools, and templates.
- (Lead CRA, if assigned) Oversee monitoring on complex studies; develop study-specific monitoring documents (e.g., CMP, deviation plan, report templates); finalize visit reports; train/coordinate CRAs; act as primary clinical monitoring contact for PM/Sponsor and handle CRA escalations.
What You'll Need:
- Bachelor's degree (life sciences, nursing, or related field preferred)
- 5-7+ years' experience conducting on-site and remote monitoring visits (or equivalent clinical research experience)
- Senior CRA levelling: SCRA I (3-5 yrs) - independently manages complex sites; SCRA II (5+ yrs) - oversees complex sites/regions, mentors peers, and drives process improvements
- Broad therapeutic exposure across multiple study types and indications
- Strong technical/scientific aptitude with the ability to quickly grasp and execute clinical protocols
- Advanced organizational and logistical skills; able to manage multiple sites/protocols within budget and timelines
- Excellent written and verbal communication; confident stakeholder engagement
- Solid understanding of medical/therapeutic areas and medical terminology
- Proven ability to train, coach, and mentor clinical research staff
- Proficient with MS Office and EDC systems; willing to travel up to 80%
- Ability to remain in a stationary position for extended periods as part of normal day-to-day activities, with reasonable accommodations considered where appropriate
Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia.
What We Offer:
Medical, dental, and vision insurance
FSA, HSA
Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
Group short-term and long-term disability insurance
Group Life Insurance
401K safe harbor plan and company match
Paid vacation, holiday, sick and volunteer time
Paid maternity & paternity leave
What Sets Us Apart:
WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.
We're Committed to Our Team:
WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.
How We Work at WEP Clinical:
At WEP Clinical, we look for individualswho are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.
Our Services Include:
Access Programs
Clinical Trial Services
Patient Site Solutions
Clinical Trial Supply
Market Access and Commercialization
Data Privacy Notice:
WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.
Privacy Policy: https://www.wepclinical.com/privacy-policy/
Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn's Easy Apply option. Please ensure your resume is in English.
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.
For Your Safety, Please Note:
We will nevercommunicate with you via Microsoft Teams or text message
We will never ask for your bank account information at any stage of recruitment
WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.
WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
#LI-fulltime #LI-remote
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About WEP Clinical
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Morrisville, NC, US
Year founded
2008