Research Assistant (Clinical)- temporary role
Behavioral Health Market Context
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Job Description
sion and documentation
• Prepare exam rooms and maintain clinical supplies for study visits
• Assist with participant flow during research visits and ensure patient comfort and safety
Research & Data Responsibilities
• Accurately enter clinical and study data into electronic data capture (EDC) systems and/or study databases
• Maintain source documentation that is complete, accurate, and audit‑ready
• Assist with informed consent discussions and documentation, as directed
• Support study visits, screenings, and follow‑ups according to protocol schedules
• Identify and promptly report protocol deviations, adverse events, and data discrepancies to the study team
Compliance & Operations
• Follow GCP, IRB, HIPAA, and institutional policies
• Assist with study regulatory binders and document maintenance
• Participate in monitoring visits, audits, and inspections as needed
• Maintain required certifications and training
Required Qualifications
• Hands‑on clinical experience performing:
• Vital signs
• Venipuncture / blood draws
• Laboratory specimen processing
• ECGs
• High school diploma or equivalent required; Associate’s or Bachelor’s degree in health sciences, life sciences, or related field preferred
• Prior experience in clinical research, healthcare, or medical assistant roles
• Strong attention to detail and documentation accuracy
• Basic computer proficiency and data entry experience
• Ability to work independently and as part of a multidisciplinary team
Preferred Qualifications
• Medical Assistant certification (CMA, RMA, or equivalent)
• GCP certification
• Experience with EDC/eSource systems (e.g., CRIO, Medidata)
• Prior experience in industry‑sponsored clinical trials
• Phlebotomy certification
Physical & Work Requirements
• Ability to stand, walk, and perform clinical procedures for extended periods
• Ability to lift and move supplies (up to 25 lbs)
• Comfortable working in a fast‑paced clinical environment
• Prepare exam rooms and maintain clinical supplies for study visits
• Assist with participant flow during research visits and ensure patient comfort and safety
Research & Data Responsibilities
• Accurately enter clinical and study data into electronic data capture (EDC) systems and/or study databases
• Maintain source documentation that is complete, accurate, and audit‑ready
• Assist with informed consent discussions and documentation, as directed
• Support study visits, screenings, and follow‑ups according to protocol schedules
• Identify and promptly report protocol deviations, adverse events, and data discrepancies to the study team
Compliance & Operations
• Follow GCP, IRB, HIPAA, and institutional policies
• Assist with study regulatory binders and document maintenance
• Participate in monitoring visits, audits, and inspections as needed
• Maintain required certifications and training
Required Qualifications
• Hands‑on clinical experience performing:
• Vital signs
• Venipuncture / blood draws
• Laboratory specimen processing
• ECGs
• High school diploma or equivalent required; Associate’s or Bachelor’s degree in health sciences, life sciences, or related field preferred
• Prior experience in clinical research, healthcare, or medical assistant roles
• Strong attention to detail and documentation accuracy
• Basic computer proficiency and data entry experience
• Ability to work independently and as part of a multidisciplinary team
Preferred Qualifications
• Medical Assistant certification (CMA, RMA, or equivalent)
• GCP certification
• Experience with EDC/eSource systems (e.g., CRIO, Medidata)
• Prior experience in industry‑sponsored clinical trials
• Phlebotomy certification
Physical & Work Requirements
• Ability to stand, walk, and perform clinical procedures for extended periods
• Ability to lift and move supplies (up to 25 lbs)
• Comfortable working in a fast‑paced clinical environment
Qualifications
- •Hands‑on clinical experience performing:
- •Vital signs
- •Venipuncture / blood draws
- •Laboratory specimen processing
- •ECGs
- •Prior experience in clinical research, healthcare, or medical assistant roles
- •Strong attention to detail and documentation accuracy
- •Basic computer proficiency and data entry experience
- •Ability to work independently and as part of a multidisciplinary team
- •Physical & Work Requirements
- •Ability to stand, walk, and perform clinical procedures for extended periods
- •Ability to lift and move supplies (up to 25 lbs)
- •Comfortable working in a fast‑paced clinical environment
Benefits
Responsibilities
- •Clinical & Patient‑Facing Duties
- •Obtain and document vital signs (blood pressure, heart rate, temperature, respiratory rate, height, weight) per protocol
- •Perform venipuncture and blood draws for research studies
- •Process, label, centrifuge, store, and ship laboratory specimens according to protocol and laboratory manuals
- •Perform 12‑lead ECGs and ensure accurate transmission and documentation
- •Prepare exam rooms and maintain clinical supplies for study visits
- •Assist with participant flow during research visits and ensure patient comfort and safety
- •Research & Data Responsibilities
- •Accurately enter clinical and study data into electronic data capture (EDC) systems and/or study databases
- •Maintain source documentation that is complete, accurate, and audit‑ready
- •Assist with informed consent discussions and documentation, as directed
- •Support study visits, screenings, and follow‑ups according to protocol schedules
- •Identify and promptly report protocol deviations, adverse events, and data discrepancies to the study team
- •Compliance & Operations
- •Follow GCP, IRB, HIPAA, and institutional policies
- •Assist with study regulatory binders and document maintenance
- •Participate in monitoring visits, audits, and inspections as needed
- •Maintain required certifications and training
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