Clinical Trials Coordinator: Patient Care & Data Integrity

Medix; Framingham (MA); On-site; USD 44,000 - 47,000; Full time

Job summary

Medix is seeking a Clinical Research Coordinator in Framingham, MA to support clinical trials on a contract-to-hire basis. The role includes participant screening, scheduling and data entry, with oversight of regulatory documents and trial logs.

The ideal candidate will have 2–3 years of clinical research experience, familiarity with GCP/IATA/FDA regulations, and fluent English. Training on protocols, IRB documentation, and trial systems is provided.

Qualifications

• 2–3 years within clinical research.
• College degree in health sciences or significant relevant experience preferred.
• Fluent in written and spoken English.
• Knowledge of GCP, IATA and FDA regulations pertaining to clinical trials.

Responsibilities

• Pre-screen, recruit and schedule participants.
• Complete protocol and trial system training.
• Maintain regulatory documents and study files.
• Obtain informed consent and discuss the study with participants.
• Enter data in the EDC and resolve queries.
• Monitor visits and address issues promptly.
• Manage and report AEs/SAEs and deviations.
• Maintain inventory of study supplies and coordinate payments to participants.
• Ensure regulatory information (IRB docs, disclosures, CVs, trainings) is up to date.

Skills

Clinical research

GCP knowledge

IATA knowledge

FDA regulations

Fluent English

Education

Bachelor's degree in health sciences

Job description

Medix is seeking a Clinical Research Coordinator in Framingham, MA to support clinical trials on a contract-to-hire basis. The role includes participant screening, scheduling and data entry, with oversight of regulatory documents and trial logs.

The ideal candidate will have 2–3 years of clinical research experience, familiarity with GCP/IATA/FDA regulations, and fluent English. Training on protocols, IRB documentation, and trial systems is provided.