Job Summary
The Clinical Research Associate I (CRA I) plays a crucial role in the clinical research process by ensuring compliance with regulatory requirements and company standards. The individual in this position assists in the management of clinical trials and collaborates with various stakeholders to uphold the integrity of data collection and reporting. This entry-level role is ideal for those looking to gain experience in clinical research while contributing to the advancement of medical science.
Responsibilities
- Monitor and oversee the progress of clinical trials, ensuring adherence to protocols and safety standards.
- Assist in the selection and initiation of study sites and investigators for clinical trials.
- Conduct routine site visits to evaluate the processes and procedures of data collection.
- Maintain accurate and complete documentation of study-related activities.
- Coordinate with site personnel, providing guidance and support on study protocols.
- Participate in training sessions for site staff on study requirements.
- Ensure timely reporting of adverse events and serious adverse events as mandated by regulations.
- Collaborate with cross-functional teams to facilitate the successful execution of clinical trials.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Strong understanding of clinical research and Good Clinical Practice (GCP) guidelines.
- Excellent organizational and communication skills.
- Ability to work independently as well as part of a team.
- Proficiency with data management systems and electronic documentation.
- Detail-oriented with strong analytical skills.
