Infectious Disease Research Coordinator

Medasource; Baltimore (MD); On-site; USD 48,000 - 55,000; Full time

Job summary

Medasource in Baltimore, MD seeks an experienced Clinical Research Coordinator to support infectious disease trials, including HIV, HBV, and HDV, with emphasis on hepatitis-focused studies.

This 3-month contract role requires independent, hands-on management of study operations, regulatory compliance, participant recruitment, and coordination with investigators, sponsors, IRBs, and study sites.

Qualifications

• Bachelor's degree in a related field.
• 3–5 years of clinical research coordination experience.
• Proven ability to manage trials with minimal supervision.
• Experience with regulatory submissions and study documentation.
• Strong organizational, communication, and problem-solving skills.

Responsibilities

• Independently coordinate daily clinical research activities to ensure protocol and regulatory compliance.
• Manage participant recruitment, screening, consent, scheduling, and study communication.
• Serve as a liaison among participants, investigators, sponsors, IRBs and stakeholders.
• Independently handle IRB submissions, amendments, continuing reviews, and regulatory correspondence.
• Maintain accurate study documentation and data entry to support data integrity.
• Support trial operations, including initiation visits, multisite coordination, and ongoing management.
• Assist with operational budget tracking and study-related administration.
• Coordinate infusion- and injection-based workflows and medication administration as feasible.
• Identify and resolve study challenges with minimal supervision.
• Learn and adapt to existing protocols to ensure continuity of activities.
• Ensure compliance with institutional policies and Good Clinical Practice (GCP).

Education

Bachelor's degree in a related field

Job description

Medasource in Baltimore, MD seeks an experienced Clinical Research Coordinator to support infectious disease trials, including HIV, HBV, and HDV, with emphasis on hepatitis-focused studies.

This 3-month contract role requires independent, hands-on management of study operations, regulatory compliance, participant recruitment, and coordination with investigators, sponsors, IRBs, and study sites.