Clinical Research Coordinator
25–35 an hour
Behavioral Health Market Context
Apply Nowvia Actalent Careers
Benefits
Health InsurancePaid Time OffDental Coverage
Job Description
nce, strong organizational skills, and the ability to engage confidently with participants and research staff.
Key Responsibilities
Participant Recruitment & Screening
• Identify, recruit, and prescreen potential participants for eligibility.
• Conduct phone screenings and review inclusion/exclusion criteria.
• Perform thorough reviews of patient medical records to determine suitability.
• Build and maintain relationships with referral physicians to support recruitment.
Data & Documentation Management
• Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy.
• Resolve EDC data queries promptly.
• Retrieve necessary medical records and ensure proper documentation.
Qualifications
Clinical Research Experience: Previous experience as a Clinical Research Coordinator is required.
Technical Proficiency: Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.
Communication Skills: Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members.
Attention to Detail: Demonstrated accuracy in documentation, data entry, and protocol adherence.
Job Type & Location
This is a Contract position based out of Leesburg, VA.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Leesburg,VA.
Application Deadline
This position is anticipated to close on Apr 15, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.
Key Responsibilities
Participant Recruitment & Screening
• Identify, recruit, and prescreen potential participants for eligibility.
• Conduct phone screenings and review inclusion/exclusion criteria.
• Perform thorough reviews of patient medical records to determine suitability.
• Build and maintain relationships with referral physicians to support recruitment.
Data & Documentation Management
• Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy.
• Resolve EDC data queries promptly.
• Retrieve necessary medical records and ensure proper documentation.
Qualifications
Clinical Research Experience: Previous experience as a Clinical Research Coordinator is required.
Technical Proficiency: Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.
Communication Skills: Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members.
Attention to Detail: Demonstrated accuracy in documentation, data entry, and protocol adherence.
Job Type & Location
This is a Contract position based out of Leesburg, VA.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Leesburg,VA.
Application Deadline
This position is anticipated to close on Apr 15, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.
Qualifications
- •The ideal candidate has hands-on clinical research experience, strong organizational skills, and the ability to engage confidently with participants and research staff
- •Clinical Research Experience: Previous experience as a Clinical Research Coordinator is required
- •Technical Proficiency: Experience with electronic medical records (EMR) and electronic data capture (EDC) systems
- •Communication Skills: Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members
- •Maintaining an inclusive environment through persistent self-reflection
Benefits
- •Pay and Benefits
- •The pay range for this position is $25.00 - $35.00/hr
- •subject to specific elections, plan, or program terms
- •Medical, dental & vision
- •Critical Illness, Accident, and Hospital
- •401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- •Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- •Short and long-term disability
- •Health Spending Account (HSA)
- •Transportation benefits
- •Employee Assistance Program
- •Time Off/Leave (PTO, Vacation or Sick Leave)
- •Ensuring growth opportunities for our people
Responsibilities
- •Schedule: 30 hours per week, Monday–Friday during standard business hours
- •We are seeking a detail‑oriented and proactive Clinical Research Coordinator (CRC) to support an ongoing clinical trial
- •Identify, recruit, and prescreen potential participants for eligibility
- •Conduct phone screenings and review inclusion/exclusion criteria
- •Perform thorough reviews of patient medical records to determine suitability
- •Build and maintain relationships with referral physicians to support recruitment
- •Data & Documentation Management
- •Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy
- •Resolve EDC data queries promptly
- •Retrieve necessary medical records and ensure proper documentation
- •Attention to Detail: Demonstrated accuracy in documentation, data entry, and protocol adherence
- •Building a culture of care, engagement, and recognition with clear outcomes
More Jobs
- Remote Board Certified Behavior Analyst (BCBA)- Supporting ABA Centers in NCat Autism 360
- Clinical Trials Assistant Coordinator - Research Supportat Rehabilitation and Neurological Services, LLC
- Clinical Trials for Moneyat Care Health
- BCBA - Flexible, Impactful Autism Services (Remote/Hybrid)at Key Autism Services
- Hiring BCBA Roles at Team PBSat Positive Behavior Supports Corporation
- LMFT | Ankeny, Iowaat ProCare Therapy
- ID 6619 - Speech Language Pathologist - 1.0 FTE for 191 days/yearat Lake Oswego Public Schools
- Board Certified Behavior Analystsat Akoya Behavioral Health
- Atlantic Behavioral Excellenceat BK Behavior
- Hiring BCBA Roles at Team PBSat Positive Behavior Supports Corporation