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Title
Text copied to clipboard!Clinical Research Coordinator
Description
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We are looking for a Clinical Research Coordinator to join our dynamic research team. The ideal candidate will be responsible for overseeing and managing clinical trials and research studies from initiation to completion. This role involves working closely with principal investigators, sponsors, regulatory bodies, and study participants to ensure that all clinical research activities are conducted in compliance with regulatory requirements and institutional policies.
As a Clinical Research Coordinator, you will be responsible for recruiting and enrolling study participants, obtaining informed consent, scheduling study visits, collecting and managing data, and ensuring the integrity and accuracy of research documentation. You will also be responsible for monitoring patient safety, reporting adverse events, and maintaining communication with all stakeholders involved in the research process.
The successful candidate should have a strong understanding of clinical research protocols, Good Clinical Practice (GCP) guidelines, and ethical standards. Attention to detail, excellent organizational skills, and the ability to work independently and collaboratively are essential for this role. Prior experience in clinical research or a related healthcare field is highly desirable.
This position offers an exciting opportunity to contribute to cutting-edge medical research and to play a vital role in advancing healthcare through evidence-based studies. If you are passionate about clinical research and committed to improving patient outcomes, we encourage you to apply.
Responsibilities
Text copied to clipboard!- Coordinate and manage clinical research studies and trials.
- Recruit and enroll study participants according to protocol.
- Obtain informed consent and maintain accurate documentation.
- Schedule and conduct study visits and follow-ups.
- Collect, process, and manage clinical data.
- Ensure compliance with regulatory and ethical guidelines.
- Monitor patient safety and report adverse events.
- Maintain communication with investigators, sponsors, and IRBs.
- Prepare and submit regulatory documents and reports.
- Assist in budget preparation and study billing.
- Train and supervise research assistants or interns.
- Participate in audits and quality assurance activities.
Requirements
Text copied to clipboard!- Bachelor’s degree in life sciences, nursing, or related field.
- Certification as a Clinical Research Coordinator (preferred).
- Minimum 2 years of experience in clinical research.
- Knowledge of GCP, FDA regulations, and IRB processes.
- Strong organizational and time management skills.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office and data management systems.
- Ability to work independently and in a team environment.
- Attention to detail and problem-solving abilities.
- Experience with electronic data capture systems (e.g., REDCap).
- Ability to handle confidential information with discretion.
- CPR certification (preferred).
Potential interview questions
Text copied to clipboard!- Do you have experience coordinating clinical research studies?
- Are you certified as a Clinical Research Coordinator?
- How do you ensure compliance with GCP and regulatory guidelines?
- Can you describe your experience with patient recruitment?
- What data management systems have you used in past roles?
- How do you handle adverse event reporting?
- Describe a challenging situation in a clinical trial and how you resolved it.
- Are you comfortable working with diverse patient populations?
- What strategies do you use to maintain accurate documentation?
- Have you participated in any clinical research audits?
- What is your availability to start this position?
- Do you have experience training or supervising research staff?
