Research Study Coordinator Research - Clinical Trials, Full-time, Day
About The Position
Coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research; acts as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the PI and the protocol, and coordinates all activities specifically related to the implementation of the treatment regimen, including consenting subjects when appropriate, scheduling appointments and ancillary services, registering patients for billing compliance and data collection. Remains current in all regulatory education, training and certification requirements.
Requirements
- Bachelor`s degree or minimum ten years' experience as a study coordinator required
- Utilizes computer programs, software, excel, web-based databases and data entry
- Medical terminology required
- Full range of body motion including physically assisting patients, requiring stretching, bending, lifting, sitting, kneeling, stooping, standing, walking, pushing and pulling
- Exerting in excess of 100 pounds of force occasionally, and/or in excess of 50 pounds of force frequently, and/or in excess of 20 pounds of force constantly to move objects
- Manual and finger dexterity and hand-eye coordination
- Constant talking and listening in English
- Effective oral and written communication skills, including speech clarity, understanding the information relayed
- Deductive and inductive reasoning skills
- Considerable walking, standing, sitting, reaching, filing, typing and photocopying required
- Ability to perform work accurately and pay attention to details, often changing from one task to another without loss of efficiency or composure
- Ability to function competently in stressful situations and changing work environment related to changing needs of patients with acute, chronic and/or complex and/or terminal disease processes
- Ability to work cooperatively within health system, multidisciplinary team members (i.e. MDs, Nurses, Rehab, Respiratory, DI, Laboratory, etc)
- Ability to utilize effective time management skills to set priorities to perform responsibilities, problem solve and deliver care
Nice To Haves
- CPR
- Phlebotomy
- IATA
- CCRP or CCRC certification upon hire or to be obtained as appropriate
- Maintains CITI certification and ongoing knowledge of ICH-GCP
Responsibilities
- Coordinates and administers research study associated activities
- Assists in project planning
- Coordinates and implements clinical research
- Acts as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the PI and the protocol
- Coordinates all activities specifically related to the implementation of the treatment regimen, including consenting subjects when appropriate, scheduling appointments and ancillary services, registering patients for billing compliance and data collection
- Remains current in all regulatory education, training and certification requirements
Benefits
- Medical/Prescription
- Dental & Vision Discount Program (Full Time/Part Time Employees)
- Group Term Life Insurance and AD&D(Full Time Employees)
- Flexible Spending Accounts
- Commuter Benefit Plans
- Supplemental Voluntary Benefits (e.g. Short-term and Long-term Disability, Whole Life Insurance, Legal Support, etc.)
- 6 Paid Holidays
- Paid Time Off (varies)
- Wellness Time Off
- Extended Illness
- Retirement Plan
- Tuition Assistance
- Employee Assistance Program (EAP)
- Valley Health LifeStyles Fitness Center Membership Discount
- Day Care Discounts for Various Daycare Facilities
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
