Dynamic Clinical Research Coordinator II

Dm Clinical Research Group; Bay City (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Dm Clinical Research Group in Bay City, Michigan seeks a proactive Clinical Research Coordinator II to ensure quality research at assigned sites in line with sponsor protocols, FDA regulations, and ICH/GCP guidelines.

You will conduct subject visits, manage documentation to ALCOA-C standards, and coordinate with laboratory, data, admin staff, investigators, and sponsor representatives. Strong English communication and multitasking are essential, with bilingual English/Spanish preferred.

Qualifications

• High School Diploma or equivalent required; Bachelor's degree preferred.
• Foreign Medical Graduates preferred.
• At least 2 years of CRC experience, preferably with practice coordinating industry-sponsored vaccines in a private setting.
• ACRP certification is preferred.
• Proficient English communication; bilingual English/Spanish preferred.

Responsibilities

• Conduct study subject visits and document procedures as per protocol.
• Adhere to ALCOA-C standards in all study documentation.
• Complete data entry and resolve queries per internal guidelines and sponsor expectations.
• Coordinate with Laboratory, Data, Administrative staff, Investigators, Research Participants, and Sponsor/CRO representatives.
• Conduct patient consent discussions and ensure comprehension before obtaining consent.
• Facilitate communication between patients, healthcare providers, and research staff.
• Attend Investigator Meetings as required.

Skills

Attention to detail

Multi-tasking

Communication skills

Bilingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree preferred

Foreign Medical Graduates preferred

Job description

Dm Clinical Research Group in Bay City, Michigan seeks a proactive Clinical Research Coordinator II to ensure quality research at assigned sites in line with sponsor protocols, FDA regulations, and ICH/GCP guidelines.

You will conduct subject visits, manage documentation to ALCOA-C standards, and coordinate with laboratory, data, admin staff, investigators, and sponsor representatives. Strong English communication and multitasking are essential, with bilingual English/Spanish preferred.