Job Description

Job Type

Part-time

Description

Compensation: $33 per hour

Location: Akron, Ohio - On-site
Reports To: Principal Investigator / Clinical Operations Manager

Position Overview

The Clinical Research Coordinator (CRC) manages and coordinates clinical trials following regulatory standards, study protocols, and ethical guidelines. The CRC ensures participant safety, safeguards data integrity, and facilitates the smooth conduct of clinical studies. This role demands strong organizational skills, attention to detail, and ongoing collaboration with investigators, research teams, and sponsors.

Essential Functions

• Manage all elements of clinical trials, including recruiting participants, enrolling them, and conducting follow-ups.
• Ensure adherence to study protocols, ICH-GCP guidelines, and applicable regulatory requirements (FDA, EMA).
• Maintain accurate and timely documentation in study records, electronic data capture (EDC) systems, and regulatory files.
• Schedule and perform study visits, assessments, and procedures as specified in the protocol.
• Collect, process, and manage study data while ensuring quality and confidentiality. Collaborate with investigators, sponsors, and multidisciplinary teams to achieve study objectives.
• Monitor study progress and promptly report deviations, adverse events, or other issues.
• Engage in training and ongoing professional development to stay updated on clinical research standards.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, or a related field.
• Clinical research experience is preferred but not required for entry-level applicants.
• Knowledge of clinical trial procedures, regulatory compliance, and patient safety principles
• Strong organizational, analytical, and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office Suite; familiarity with EDC or CTMS systems is a plus.
• Strong focus on detail and commitment to data accuracy
• Able to handle multiple tasks and prioritize effectively. Collaborative-comfortable working with diverse teams.
• Ethical judgment and a strong understanding of confidentiality in clinical research

Adaptability and eagerness to learn in a rapidly changing environment

Work Environment & Travel

• Part-time position
• Occasional travel to clinical sites or training sessions might be necessary.

Compensation
• Competitive salary based on experience and qualifications
• To Apply:
Visit and navigate to the Careers Page to submit your resume and a brief cover letter outlining your interest and qualifications. Applications will be reviewed on a rolling basis.

SerenaGroup is committed to fostering a diverse and inclusive workplace. All qualified candidates will be considered for employment.

Salary Description

33 per hour

Job Tags

Hourly pay, Full time, Part time, Work at office,

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