Duties:
- Coordination of study protocols under the direction of the Principal Investigator
- Patient-related procedures such as: scheduling and completing participant visits using source documents; vitals, height, weight and ECG collection, phlebotomy/specimen collection; serving as the first point of contact for participant concerns; working with investigational products
- Data entry and maintaining study files
- Communicating with sponsors and meeting sponsor demands
- Traveling for new study start-up up to 4x/year
- The type of employee we are looking for:
- Organized and able to handle fast-paced, occasionally stressful situations
- Calm under pressure and capable of solving sudden problems that may not have clear answers or readily available resources
- Personable
- Trusted to work independently
- An effective communicator who can cooperate as a member of a team
- Ability to prioritize and multitask
- Ability to work within a hierarchy
Qualifications
Required:
- BS/BA, RN, or higher
- Ability to navigate technology and programs independently and adeptly
- COVID-19 Vaccination
- Must be able to commute to both West Chester, PA and Media, PA
Preferred, but not necessary:
- Experience in clinical research
- Background in behavioral techniques, such as a case management worker or therapeutic staff support
Job Type: Full-time
Pay: From $40,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible schedule
- Health insurance
- Paid time off
- Parental leave
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Application Question(s):
- Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)?
- Are you able to work at two different office locations, West Chester, PA and Media, PA?
Education:
Experience:
- Clinical research: 1 year (Preferred)
Willingness to travel:
Work Location: Multiple locations