Clinical Research Coordinator
Behavioral Health Market Context
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Job Description
ommunity, and ensuring compliance with the highest standards of patient care.
Key Responsibilities
• Conduct intricate clinical procedures, including ECG, spirometry, sample collection, and assessing vital signs.
• Perform phlebotomy to facilitate sample collection as required.
• Coordinate clinical research studies while adhering to study protocols and Good Clinical Practice (GCP) guidelines.
• Engage with patients by conducting consenting and study visits according to established protocols.
• Process laboratory samples and conduct ambulatory blood pressure monitor (ABPM) procedures.
• Support study execution by preparing necessary materials, setting up equipment, and managing logistical details.
• Recruit, screen, and orient volunteers, ensuring their comfort and safety throughout the study.
• Collect and accurately document clinical data in case report forms (CRFs); ensure timely and precise data entry.
• Collaborate with investigators and monitors, addressing inquiries and maintaining data quality.
• Act as an advocate for volunteers, ensuring a safe environment in line with Health and Safety policies.
Qualifications
• High School Diploma or equivalent education and experience.
• At least 1 year of relevant experience in clinical research is preferred.
• Familiarity with clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to build effective working relationships.
• Capability to assist in patient recruitment efforts, including phone prescreening and chart review.
• Aptitude for assisting with data entry and query resolution.
• Willingness to support patient visits effectively.
Please note: This position is not eligible for sponsorship.
This role is based in Malden, MA. Become part of a leading global provider of clinical research services that accelerates the development of innovative medical treatments, and help enhance patient outcomes and population health worldwide.
Compensation: The potential base pay range for this role is $35.00 to $42.00 per hour, with actual pay depending on various factors, including qualifications, experience, and location.
Key Responsibilities
• Conduct intricate clinical procedures, including ECG, spirometry, sample collection, and assessing vital signs.
• Perform phlebotomy to facilitate sample collection as required.
• Coordinate clinical research studies while adhering to study protocols and Good Clinical Practice (GCP) guidelines.
• Engage with patients by conducting consenting and study visits according to established protocols.
• Process laboratory samples and conduct ambulatory blood pressure monitor (ABPM) procedures.
• Support study execution by preparing necessary materials, setting up equipment, and managing logistical details.
• Recruit, screen, and orient volunteers, ensuring their comfort and safety throughout the study.
• Collect and accurately document clinical data in case report forms (CRFs); ensure timely and precise data entry.
• Collaborate with investigators and monitors, addressing inquiries and maintaining data quality.
• Act as an advocate for volunteers, ensuring a safe environment in line with Health and Safety policies.
Qualifications
• High School Diploma or equivalent education and experience.
• At least 1 year of relevant experience in clinical research is preferred.
• Familiarity with clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to build effective working relationships.
• Capability to assist in patient recruitment efforts, including phone prescreening and chart review.
• Aptitude for assisting with data entry and query resolution.
• Willingness to support patient visits effectively.
Please note: This position is not eligible for sponsorship.
This role is based in Malden, MA. Become part of a leading global provider of clinical research services that accelerates the development of innovative medical treatments, and help enhance patient outcomes and population health worldwide.
Compensation: The potential base pay range for this role is $35.00 to $42.00 per hour, with actual pay depending on various factors, including qualifications, experience, and location.
Qualifications
- •High School Diploma or equivalent education and experience
- •Familiarity with clinical trials, GCP principles, and medical terminology
- •Strong attention to detail and ability to build effective working relationships
- •Capability to assist in patient recruitment efforts, including phone prescreening and chart review
- •Aptitude for assisting with data entry and query resolution
- •Willingness to support patient visits effectively
Benefits
- •Compensation: The potential base pay range for this role is $35.00 to $42.00 per hour, with actual pay depending on various factors, including qualifications, experience, and location
Responsibilities
- •Schedule: Part-time, 24 hours per week
- •Join our dynamic team as a Clinical Research Coordinator (CRC) where you will play a vital role in supporting groundbreaking clinical research studies alongside an experienced principal investigator
- •This hands-on position involves performing critical clinical procedures, engaging with the community, and ensuring compliance with the highest standards of patient care
- •Conduct intricate clinical procedures, including ECG, spirometry, sample collection, and assessing vital signs
- •Perform phlebotomy to facilitate sample collection as required
- •Coordinate clinical research studies while adhering to study protocols and Good Clinical Practice (GCP) guidelines
- •Engage with patients by conducting consenting and study visits according to established protocols
- •Process laboratory samples and conduct ambulatory blood pressure monitor (ABPM) procedures
- •Support study execution by preparing necessary materials, setting up equipment, and managing logistical details
- •Recruit, screen, and orient volunteers, ensuring their comfort and safety throughout the study
- •Collect and accurately document clinical data in case report forms (CRFs); ensure timely and precise data entry
- •Collaborate with investigators and monitors, addressing inquiries and maintaining data quality
- •Act as an advocate for volunteers, ensuring a safe environment in line with Health and Safety policies