Clinical Research coordinator

Atrium Health; Rome (GA); On-site; USD 55,000 - 75,000; Full time

Job summary

Atrium Health is seeking a Clinical Research Coordinator to join our research operations in Georgia. You will lead recruitment, consent, and coordination of lab tests for study subjects, working closely with Investigational Pharmacy and sponsors to ensure smooth drug administration and billing.

You'll manage IRB documents, maintain accurate study data, and communicate with investigators, sponsors, and federal agencies.

Qualifications

• RN licensure required; BSN preferred.
• Clinical research experience preferred.
• BLS certification required per policy.
• Certification in clinical research (SoCRA, ACRP) preferred.

Responsibilities

• Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
• Coordinates with investigators to conduct appropriate laboratory tests and procedures for subjects; including blood draws.
• Coordinates with Investigational Pharmacy for subjects to receive required drugs.
• Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
• Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
• Records clinical and laboratory data on forms provided by investigators, government, and sponsors.
• Communicates with study sponsors, federal agencies, investigators, and sub-investigators about research projects.
• Provides resources for staff, patients, families, and community regarding research.
• Travels to clinical sites within the System as necessary.
• Performs other duties as assigned within department.

Skills

Clinical research coordination

Informed consent procedures

Interdepartmental communication

Education

RN licensure (applicable state)

BSN preferred

BLS certification

Certification in clinical research (SoCRA/ACRP) preferred

Job description

• Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
• Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
• Coordinates with Investigational Pharmacy for subjects to receive required drugs.
• Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
• Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
• Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.
• Communicates with study sponsors, federal agencies, principal investigators, and sub-investigators about research projects.
• Provides resources for staff, patients, families. and community regarding research.
• Travels to clinical research sites, hospitals, physician offices, and facilities within the System as necessary.
• Performs other duties as assigned within department

Essential Functions

• Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
• Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
• Coordinates with Investigational Pharmacy for subjects to receive required drugs.
• Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
• Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
• Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.
• Communicates with study sponsors, federal agencies, principal investigators, and sub-investigators about research projects.
• Provides resources for staff, patients, families. and community regarding research.
• Travels to clinical research sites, hospitals, physician offices, and facilities within the System as necessary.
• Performs other duties as assigned within department

Physical Requirements

• Requires ability to sit, stand, or walk for long periods of time. Reaching, stooping, bending in file drawers. Lifting, pushing, pulling up to 30 lbs. of weight. Working in fast-paced clinical setting. Intact sense of sight, hearing, smell, and touch and manual and finger dexterity. Must be able to be mobile within the entire healthcare system and other facilities as required

Education, Experience And Certifications

• applicable state RN licensure required; BSN preferred. Clinical research experience preferred. BLS required per policy guidelines. Certification in clinical research (SoCRA, ACRP) preferred.