Clinical Research Coordinator

search projects. This includes developing and writing protocols, conducting research activities, and monitoring the progress of research studies. The ideal candidate is a detail-oriented, organized individual with excellent communication skills and a commitment to providing quality care to our patients.The successful candidate must possess a Bachelor’s degree in a health-related field with a minimum of two years of clinical research experience. Knowledge of Good Clinical Practice (GCP) and/or the International Conference on Harmonization (ICH) guidelines is also required. Previous experience with regulatory and ethics submissions is preferred.The Clinical Research Coordinator must be able to work independently and as part of a team in a fast-paced, ever changing environment. In addition, the successful candidate must possess strong problem-solving skills and the ability to analyze data. We are looking for an individual who is driven, motivated, and has a strong commitment to patient care.

Responsibilites:

Develop and write clinical research protocols.
Conduct research activities.
Monitor progress of research studies.
Ensure adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Submit regulatory and ethics applications.
Analyze data and solve problems.
Communicate effectively with other members of the clinical research team.
Remain organized and up to date on all research projects.
Maintain a commitment to patient care.
Work independently and in a team environment.

BJC HealthCare is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.