Senior Clinical Research Coordinator: Data & Compliance

Dm Clinical Research Group; Pennsylvania; On-site; USD 60,000 - 85,000; Full time

Job summary

DM Clinical Research Group in Philadelphia, PA is seeking a Clinical Research Coordinator II to ensure quality research at assigned sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. The role also focuses on achieving enrollment targets and delivering reliable data to sponsors.

You will perform site visits, training, data entry, adverse event reporting, and liaise with investigators, staff, and sponsors.

Qualifications

• Must have CRC experience and be proficient in clinical trial documentation.
• Familiarity with ICH-GCP, FDA regulations, and sponsor protocols preferred.
• Strong communication and organizational skills required.

Responsibilities

• Conduct subject visits and protocol-specific procedures with timely documentation.
• Maintain ALCOA-C compliant records and data entries.
• Oversee adverse event reporting and safety communications to authorities.
• Coordinate training, site management, and adherence to study protocols.
• Facilitate communication among participants, investigators, and sponsor/CRO teams.
• Attend investigator meetings and ensure regulatory readiness at sites.

Skills

Communication skills

Bilingual English/Spanish

Detail oriented

Multi-tasking

Education

High School Diploma or equivalent

Bachelor's degree preferred

Job description

DM Clinical Research Group in Philadelphia, PA is seeking a Clinical Research Coordinator II to ensure quality research at assigned sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. The role also focuses on achieving enrollment targets and delivering reliable data to sponsors.

You will perform site visits, training, data entry, adverse event reporting, and liaise with investigators, staff, and sponsors.