Clinical Research Coordinator (CRC) at SerenaGroup Inc

Akron, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

02 Jan, 26

Salary

33.0

Posted On

04 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Regulatory Compliance, Patient Safety, Organizational Skills, Analytical Skills, Problem-Solving Skills, Communication Skills, Microsoft Office Suite, Data Accuracy, Collaboration, Ethical Judgment, Adaptability, Attention to Detail, Recruitment, Data Management, Training

Industry

Medical and Diagnostic Laboratories

Description

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 www.serenagroups.com 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.

Responsibilities

The Clinical Research Coordinator (CRC) manages and coordinates clinical trials, ensuring participant safety and data integrity. This role involves recruiting participants, adhering to study protocols, and collaborating with multidisciplinary teams.