Clinical Research Coordinator II — Vaccines Trials

Paycom - ATS; Minnesota; On-site; USD 60,000 - 80,000; Full time

Job summary

Paycom - ATS is seeking a CRC II to conduct site visits, manage trial documentation, and ensure data integrity across sponsor protocols. The role emphasizes regulatory compliance, ALCOA-C standards, and teamwork with Lab, Data, and Clinical staff in Minnesota.

Responsibilities include informed consent, safety reporting, data entry, and site coordination to meet enrollment and quality targets in a fast-paced research environment.

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree preferred.
• ACRP certification or equivalent preferred.
• Strong written and verbal English communication.
• Bilingual English/Spanish preferred.

Responsibilities

• Conduct study subject visits and document procedures per protocol.
• Adhere to ALCOA-C standards in all trial documentation.
• Complete data entry and query resolution per guidelines and sponsor expectations.
• Liaise with Laboratory, Data, Administrative staff, Investigators, participants and Sponsor/CRO.
• Oversee reporting of Adverse Events and safety information as required.
• Obtain informed consent and explain study procedures, risks and benefits to participants.
• Support recruitment and retention activities at assigned sites.
• Prepare for sponsor/CRO and Investigator Meetings as needed.
• Attend investigator meetings as required.

Skills

Attention to detail

Multitasking

Proficient English communication

Bilingual English/Spanish preferred

Clinical research coordination

Education

High School Diploma or equivalent

Bachelor's degree preferred

ACRP certification preferred

Job description

Paycom - ATS is seeking a CRC II to conduct site visits, manage trial documentation, and ensure data integrity across sponsor protocols. The role emphasizes regulatory compliance, ALCOA-C standards, and teamwork with Lab, Data, and Clinical staff in Minnesota.

Responsibilities include informed consent, safety reporting, data entry, and site coordination to meet enrollment and quality targets in a fast-paced research environment.