Clinical Research Coordinator - Columbia, MD
35–42 an hour
Behavioral Health Market Context
Apply Nowvia ZipRecruiter
Benefits
Health Insurance
Job Description
clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care.
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery.
What You'll Do
• Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs
• Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)
• Prepare study materials, manage logistics, and support overall site operations
• Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach
• Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria
• Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution
• Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues
• Maintain a safe environment for volunteers in alignment with Health & Safety policies
What We're Looking For
• High School Diploma or equivalent education/experience
• Minimum 1 year of relevant clinical research experience (preferred)
• Working knowledge of clinical trials, GCP principles, and medical terminology
• Strong attention to detail and ability to build effective working relationships
• Recruitment-focused with strong patient-facing experience as a Clinical Research Coordinator (CRC)
• Demonstrated knowledge of the full study lifecycle from start-up to close-out
• Hands-on experience performing CRC tasks in a clinic setting
• Skilled in patient recruitment, prescreening, and using study protocols to identify inclusion/exclusion criteria
• Proficient with Electronic Data Capture (EDC) systems and query resolution
• Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals
• Experience in both research and clinical settings
• Regulatory experience is a plus
Please Note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery.
What You'll Do
• Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs
• Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)
• Prepare study materials, manage logistics, and support overall site operations
• Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach
• Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria
• Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution
• Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues
• Maintain a safe environment for volunteers in alignment with Health & Safety policies
What We're Looking For
• High School Diploma or equivalent education/experience
• Minimum 1 year of relevant clinical research experience (preferred)
• Working knowledge of clinical trials, GCP principles, and medical terminology
• Strong attention to detail and ability to build effective working relationships
• Recruitment-focused with strong patient-facing experience as a Clinical Research Coordinator (CRC)
• Demonstrated knowledge of the full study lifecycle from start-up to close-out
• Hands-on experience performing CRC tasks in a clinic setting
• Skilled in patient recruitment, prescreening, and using study protocols to identify inclusion/exclusion criteria
• Proficient with Electronic Data Capture (EDC) systems and query resolution
• Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals
• Experience in both research and clinical settings
• Regulatory experience is a plus
Please Note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP #ONSITE
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Qualifications
- •High School Diploma or equivalent education/experience
- •Working knowledge of clinical trials, GCP principles, and medical terminology
- •Strong attention to detail and ability to build effective working relationships
- •Recruitment-focused with strong patient-facing experience as a Clinical Research Coordinator (CRC)
- •Demonstrated knowledge of the full study lifecycle from start-up to close-out
- •Hands-on experience performing CRC tasks in a clinic setting
- •Skilled in patient recruitment, prescreening, and using study protocols to identify inclusion/exclusion criteria
- •Proficient with Electronic Data Capture (EDC) systems and query resolution
- •Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals
- •Experience in both research and clinical settings
Benefits
- •The potential base pay range for this role is $35.00-$42.00 per hour
- •The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time)
- •Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits
Responsibilities
- •Schedule: Part-time (16 hours per week)
- •Shape the Future of Medicine with IQVIA!
- •Join IQVIA as a Clinical Research Coordinator (CRC) and play a vital role in supporting clinical research studies that drive meaningful innovation
- •This hands-on role blends clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care
- •Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs
- •Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)
- •Prepare study materials, manage logistics, and support overall site operations
- •Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach
- •Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria
- •Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution
- •Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues
- •Maintain a safe environment for volunteers in alignment with Health & Safety policies
More Jobs
- Physical Therapist - PRNat Therapy Management Corporation
- Registered Behavior Technician (RBT) - Glenrock, Wyomingat Soliant
- Licensed Marriage and Family Therapist - Onsite or Remote (LMFT, LMFTS, or LCMFT)at Therapymatch Inc. (DBA Headway)
- Remote Paid Study Participant – Flexible Schedule (Earn Up to $750/Week)at Apex Focus Group Inc.
- Intern Behavior Therapistat Achieve Beyond
- BCBA — Clinical Leader, Mentorship & Pathat Action Behavior Centers
- In-Home RBT: Flexible Hours & Growth Opportunitiesat Skillful Steps ABA
- Licensed Mental Health Therapist - Onsite or Onlineat Therapymatch Inc. (DBA Headway)
- Speech Therapist SLP for Home Healthat FeldCare Connects
- Work with Kids! Registered Behavior Technician (RBT) / BCAT / ABAT – Part-Timeat Behavia Therapy