JOB SUMMARY: clinical coordination of all aspects of adult and/or pediatric clinical research trials primarily sponsored by pharmaceutical companies.
Responsibilities include, but are not limited to, the following:
Clinical Support
- Performs all aspects of research related job duties in accordance with site-specific standard operating procedures
- Maintain required certifications such as IATA and GCP training
- Follow all federal, state, and local guidelines with regard to clinical trials
- Provides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilities
- Must efficiently manage own time, handle multiple demands and competing deadlines
Other
- Maintains patient confidentiality and complies with HIPAA and compliance guidelines established by the practice
- Maintains detailed knowledge of practice management and other computer software as it relates to job functions
- Attends CPR, OSHA, HIPPA, and OIG training programs if required by the practice
- Attends all regular meetings as appropriate
Supervisory Responsibilities
This job has no supervisory responsibilities.
Typical Physical Demands
Position requires full range of body motion including manual and finger dexterity and eye-hand coordination. Involves standing and walking. Employee will occasionally be asked to lift and carry items weighing up to 30 pounds. Normal visual acuity and hearing are required. Employee may work under stressful conditions. Employee may work irregular hours and be exposed to bodily fluids on a regular basis.
Typical Working Condition
Employee will have frequent exposure to communicable diseases, toxic substances, needle sticks and other conditions common to a clinic environment.
