Clinical Research Coordinator
25–35 an hour
Behavioral Health Market Context
Apply Nowvia Actalent Careers
Benefits
Dental CoveragePaid Time OffHealth Insurance
Job Description
ion as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities. The ideal candidate has hands-on clinical research experience, 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.
• Engage in community outreach by visiting clinics/hospitals, distributing recruitment materials, educating medical staff, and maintaining online recruitment portals.
• Build and maintain relationships with referral physicians to support recruitment.
Participant Interaction & Study Conduct
• Obtain informed consent from participants in accordance with regulatory and ethical standards.
• Prepare for study visits, including scheduling participants, confirming informed consent status, preparing documents, and coordinating with the research team.
• Conduct follow-up communications with participants to ensure retention and protocol compliance.
• Schedule in-person visits and follow-up appointments; send reminders and information as needed.
Qualifications
• Previous experience as a Clinical Research Coordinator is required.
• Bilingual (English/Spanish) preferred.
• Autoimmune disease clinical trial experience preferred.
• Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.
• Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members.
• Demonstrated accuracy in documentation, data entry, and protocol adherence.
Job Type & Location
This is a Contract position based out of Carlsbad, CA.
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 Carlsbad,CA.
Application Deadline
This position is anticipated to close on Apr 27, 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.
• Engage in community outreach by visiting clinics/hospitals, distributing recruitment materials, educating medical staff, and maintaining online recruitment portals.
• Build and maintain relationships with referral physicians to support recruitment.
Participant Interaction & Study Conduct
• Obtain informed consent from participants in accordance with regulatory and ethical standards.
• Prepare for study visits, including scheduling participants, confirming informed consent status, preparing documents, and coordinating with the research team.
• Conduct follow-up communications with participants to ensure retention and protocol compliance.
• Schedule in-person visits and follow-up appointments; send reminders and information as needed.
Qualifications
• Previous experience as a Clinical Research Coordinator is required.
• Bilingual (English/Spanish) preferred.
• Autoimmune disease clinical trial experience preferred.
• Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.
• Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members.
• Demonstrated accuracy in documentation, data entry, and protocol adherence.
Job Type & Location
This is a Contract position based out of Carlsbad, CA.
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 Carlsbad,CA.
Application Deadline
This position is anticipated to close on Apr 27, 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
- •Previous experience as a Clinical Research Coordinator is required
- •Experience with electronic medical records (EMR) and electronic data capture (EDC) systems
- •Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members
- •Demonstrated accuracy in documentation, data entry, and protocol adherence
- •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
- •Contract Duration: Open-ended (estimated 3–6 months)
- •Schedule: 40 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 Myasthenia Gravis clinical trial
- •This contractor will function as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities
- •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
- •Engage in community outreach by visiting clinics/hospitals, distributing recruitment materials, educating medical staff, and maintaining online recruitment portals
- •Build and maintain relationships with referral physicians to support recruitment
- •Participant Interaction & Study Conduct
- •Obtain informed consent from participants in accordance with regulatory and ethical standards
- •Prepare for study visits, including scheduling participants, confirming informed consent status, preparing documents, and coordinating with the research team
- •Conduct follow-up communications with participants to ensure retention and protocol compliance
- •Schedule in-person visits and follow-up appointments; send reminders and information as needed
- •Building a culture of care, engagement, and recognition with clear outcomes
More Jobs
- Clinical Director - BCBA at Discover Hope Behavioral Solutions Fremont, CAat Discover Hope Behavioral Solutions
- Speech Therapist-9at Raze Therapeutics
- RBT Applied Behavior Analyst Therapistat Guiding River ABA
- ABA Therapist at Kids First Services Queens, NYat Kids First Services
- Behavior Technician - Working with Childrenat Attain ABA Therapy
- IM Research Program Coordinator - Clinical Trials Opsat Texas Tech University Health Sciences Center
- School Speech and Language Pathologist | Marana, Arizonaat ProCare Therapy
- RBT/Behavioral Tech – Clinic ABA, Paid Trainingat Behavioral Innovations
- Director of Clinical Research and Real World Evidenceat Virta Health
- Behavior Technicianat Imagination ABA Therapy