Clinical Research Coordinator (CRC) I

ADP, Inc.; Baltimore (MD); On-site; USD 52,000 - 78,000; Full time

Job summary

ADP, Inc. is seeking a Clinical Research Coordinator (CRC) I to join our Baltimore, MD research team. This full-time position coordinates all aspects of assigned clinical trials, from pre-study planning through patient visits and study documentation.

The CRC will maintain protocol knowledge, manage visit schedules, ensure proper medical evaluation, and work with data management to transcribe data into eCRFs while supporting sponsor monitoring and regulatory compliance.

Qualifications

• Associate or Bachelor’s degree in related field.
• 1-2 years of clinical trials/research experience is required.

Responsibilities

• Coordinates and manages all aspects of assigned clinical trials from pre-study planning through completion of patient visits and study documentation.
• Coordinates and conducts patient/subject visit schedules and ensures appropriate medical evaluation and care.
• Works with data management to transcribe source data into eCRFs.
• Facilitates sponsor monitoring and database clean-up processes.
• Conducts clinical research in compliance with all applicable regulations, including GCPs and company SOPs.

Skills

Coordination

Attention to detail

Documentation skills

Education

Associate or Bachelor’s degree in related field

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Coordinator (CRC) I

FT-Permanent Staff Baltimore, MD USA, Baltimore, MD, US

30+ days ago Requisition ID: 1057

We are seeking a full-timeClinical Research Coordinatorto join ourBaltimore, MD Research team!

As aClinical Research Coordinator, you will be responsible for coordination of all aspects of assigned clinical trials from pre-study planning through successful completion of all patient/subject visits and study documentation; directly involved in patient/subject care and study subject’s procedures and activities.

• Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for patient/subject visits, obtaining informed consent, visit schedules, tests, procedures, laboratory information, and drug accountability requirements
• Responsible for all study documentation forms
• Coordinates and conducts patient/subjects’ visit schedules
• Assures that research participants receive appropriate medical evaluation and care
• Works with data management group to transcribe source data into eCRFs
• Facilitates sponsor monitoring and database clean-up process
• Conducts clinical research in compliance with all applicable regulations, including GCPs and company SOPs

Qualifications:

• Associate or Bachelor’s degree in related field
• 1-2 years of clinical trials/research experience is required