Clinical Research Coordinator

Position Summary :  The Clinical Research Coordinator will be responsible for overseeing all aspects of the organization's clinical research program. This is role that requires a deep understanding of clinical trial methodologies, regulatory requirements, and a commitment to maintaining the highest standards of research integrity. The ideal candidate will possess excellent leadership, communication, and organizational skills.

Qualifications

Minimum Qualifications :

To qualify you must have a Bachelor degree or equivalent in business administration, health care administration or related field.

Minimum of two years of progressively responsible project coordination experience, preferably in a research setting.

Proficiency in using various Microsoft Office applications such as Word, Excel, Access, Power Point and Outlook.

Familiar with Internet applications.

Effective oral, written, communication, interpersonal skills.

Ability to interface effectively with all levels of management and must work and communicate effectively with both internal and external customers.

Ability to work within a team environment as well as independently.

Commitment to continuous learning as required by department administration.

Ability to operate research related equipment

Ability to work and make decisions independently.

Time management skills and ability to multitask.

Ability to identify, analyze and solve problems : Ability to work well under pressure.

Preferred Qualifications :

Clinical Research Coordinator (CRC) Certification is preferred (required in some disciplines).

Knowledge of basic medical terminology is preferred.

Responsibilities :

• In this role, the successful candidate is responsible for providing moderate to advanced range of coordination of Research studies conducted within the Division.
• Coordinator will assist with the recruitment, enrollment, grant submissions, research data collection and study coordination activities
• Ensures the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA, and required obligations to patient / subject, Principal Investigator, Research Team and sponsor.
• Interfaces directly with patients / subjects and Principal Investigator in support of the clinical trials if applicable.
• Oversee the implementation of research protocols.
• Ensure research sites are well-prepared and equipped to conduct trials, including overseeing site initiation, monitoring, and close-out visits.
• Prioritize and monitor patient safety throughout all trials, ensuring adverse events are reported promptly and accurately.
• Develop and execute strategies to meet and exceed patient recruitment and enrollment targets.

Benefits