Job summary
Job post source
This job is directly from Johnson County Clin Trials (JCCT)
Job overview
The Study Coordinator at Johnson County Clin Trials is responsible for facilitating clinical studies from start to finish, ensuring successful outcomes by working closely with study subjects and the Principal Investigator.
Responsibilities and impact
The role involves coordinating clinical studies, preparing documentation, communicating with study subjects and staff, maintaining records, and ensuring compliance with regulations and protocols.
Compensation and benefits
The position offers a competitive salary, 401(k), health insurance, paid time off, and tuition reimbursement.
Experience and skills
Candidates should have 3 to 5 years of experience in a clinical research setting, a basic understanding of relevant regulations, and a bachelor's degree in a health-related field, with CRA certification required within 6 months.
Company information
Johnson County Clinical Trials specializes in clinical research and is committed to equal opportunity employment.
Company overview
Johnson County Clin Trials (JCCT) is a clinical research organization specializing in conducting Phase I-IV clinical trials for pharmaceutical and biotechnology companies. They generate revenue by partnering with sponsors to test the safety, efficacy, and market readiness of new drugs and medical devices, adhering to regulatory standards. Established to advance medical innovation, JCCT has built a reputation for its expertise in patient recruitment, data integrity, and compliance with FDA and international guidelines. Candidates should note their emphasis on collaboration, precision, and advancing healthcare solutions.
How to land this job
Position your resume to showcase your experience in clinical research, emphasizing your understanding of study protocols and regulations such as CFR, GCP, and HIPAA, as these are critical for the Study Coordinator role at Johnson County Clin Trials (JCCT).
Highlight your ability to manage study logistics, including subject enrollment, communication with Principal Investigators, and adherence to safety regulations, as these responsibilities are central to the position.
Apply through various platforms, including the JCCT corporate site and LinkedIn, to broaden your application reach and visibility for the Study Coordinator role.
Connect with professionals in the research division at JCCT on LinkedIn to inquire about the position; potential ice breakers could include asking about their experiences with specific studies or expressing your interest in the impact of their research work.
Optimize your resume for ATS systems by incorporating keywords from the job description such as 'clinical research,' 'study protocols,' and 'informed consent' to enhance the chances of passing initial screenings.
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