Summary
The Clinical Research Coordinator is responsible for coordinating all aspects of clinical research studies, from study design and protocol development to data collection and analysis. The Clinical Research Coordinator will also work closely with study participants, investigators, and regulatory agencies to ensure that studies are conducted in a safe and ethical manner.
Responsibilities
- Screening and enrolling participants in clinical trials. This includes reviewing participant eligibility criteria, obtaining informed consent, and scheduling study visits.
- Collecting and managing clinical data. This includes ensuring that data is collected accurately and in a timely manner, and maintaining the confidentiality of participant data.
- Monitoring participant safety. This includes ensuring that participants are not experiencing any adverse events, and reporting any safety concerns to the study sponsor.
- Administering study medications and treatments. This includes ensuring that participants are receiving the correct medications and treatments, and monitoring for any side effects.
- Coordinating with other study personnel. This includes working with study nurses, data managers, and statisticians to ensure that the study is running smoothly.
- Preparing and submitting study reports. This includes preparing reports for the study sponsor, regulatory agencies, and other stakeholders.
- Training and supervising research staff. This includes providing training on clinical research procedures and ensuring that staff are following all applicable regulations.
- Providing support to study participants. This includes answering questions, providing emotional support, and helping participants navigate the clinical research process.
- Advocating for the rights of study participants. This includes ensuring that participants are treated fairly and that their rights are protected.
Qualifications
- Bachelor’s degree in a related field, such as biology, biochemistry, or nursing
- Experience in clinical research
- Strong organizational and time management skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Proficient in Microsoft Office Suite.
Skills
- Strong understanding of clinical research principles and practices
- Excellent organizational and time management skills
- Excellent written and verbal communication skills
- Ability to work independently and as part of a team
- Experience with regulatory compliance.