Job Description

Job Description

Job Description

Job Summary:

The Clinical Research Coordinator (CRC) will manage and coordinate all aspects of clinical trials and research studies. This role involves working closely with principal investigators, research staff, and participants to ensure studies are conducted according to protocol, regulatory requirements, and institutional policies. The CRC plays a critical role in the successful execution of clinical research studies.

Key Responsibilities:

Study Coordination:

· Coordinate and manage clinical trials and research studies from initiation through to completion.

· Develop and implement recruitment strategies to enroll participants in the study.

· Screen, recruit, and consent study participants according to study protocols.

Protocol Compliance:

· Ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.

· Maintain up-to-date knowledge of all regulatory requirements and ensure compliance.

Data Management:

· Collect, process, and maintain accurate study data and documentation.

· Enter data into electronic databases and ensure data integrity and quality.

· Prepare and maintain source documents, case report forms, and other required study documentation.

Participant Interaction:

· Conduct study visits, including obtaining informed consent, collecting samples, and administering questionnaires.

· Monitor participants’ adherence to study protocols and report any adverse events.

Communication:

· Serve as the primary point of contact between participants, investigators, and sponsors.

· Communicate effectively with study participants, answering questions and providing support throughout the study.

Regulatory Compliance:

· Prepare and submit study-related documents to Institutional Review Boards (IRBs) and other regulatory bodies.

· Ensure all study activities are conducted in accordance with IRB-approved protocols.

Project Management:

· Develop and maintain study timelines and ensure milestones are met.

· Coordinate study meetings and communicate updates to the research team.

Qualifications:

Education:

· Bachelor’s degree in a related field (e.g., nursing, life sciences, public health). Advanced degree preferred.

Experience:

· Experience in clinical research coordination or a related field.

· Knowledge of GCP, FDA regulations, and clinical trial processes.

Skills:

· Excellent organizational and time-management skills.

· Strong attention to detail and problem-solving abilities.

· Effective communication and interpersonal skills.

· Proficiency in Microsoft Office and clinical trial management systems (such as RealTime, etc.)

Additional Requirements:

· Certification as a Clinical Research Coordinator (CCRC) or similar is preferred.

· Ability to work independently and as part of a team.

· Flexibility to adapt to changing priorities and assignments.

· Ability to handle confidential information with discretion.

· Ability to travel to various clinical sites as required.

INNOVACORE Center for Research & Biotechnology is an equal opportunity employer and welcomes applicants from all backgrounds. We thank all applicants for their interest; however, only those shortlisted for an interview will be contacted. To learn more about INNOVACORE, please visit this website:

Company Description

INNOVACORE Center for Research & Biotechnology is an equal opportunity employer and welcomes applicants from all backgrounds. We thank all applicants for their interest; however, only those shortlisted for an interview will be contacted. To learn more about INNOVACORE, please visit this website:

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