Description
Duties:The Clinical Program Manager is responsible for leading the planning and execution of all operational aspects of clinical research in multiple therapeutic areas, which encompasses multiple studies/projects. This position works closely with various cross-functional partners both internally and externally, including medical and scientific personnel. Responsibilities include assisting the Director of Clinical Affairs in developing the clinical strategy and will lead the execution of the plans to ensure that all study operational activities are conducted efficiently, meet enrollment goals and are in compliance with all applicable regulations and Corporate SOP's.
Requirements:
- Minimum of 6 years clinical research experience in the medical device (preferred) or pharmaceutical industry
- Minimum of 3 years clinical trial management experience, demonstrated efficiency in partnering with CROs and vendors, and excellent working knowledge of GCP, ICH, and global regulations
- Bachelor's to advanced degree in biologic science or other related field and specific experience in cardiovascular or pulmonary diseases is preferred.
- Excellent communication, interpersonal, organizational skills, attention to detail, strong team player and the ability to interact positively with all levels or staff are required.
- Strong project management skills including the ability to handle multiple assignments, and work proactively and efficiently in a fast-paced, high change environment.
- Must be adept at developing and implementing metrics, clinical study patient recruitment strategies and exhibit strong presentation skills.
To find out more about Real please visit www.realstaffing.com