In a patient centric and fast paced, high volume environment, the Project Manager is responsible to manage all clinical trial milestones to ensure the delivery of quality clinical trial management services. Depending on the needs of the Sponsor or demands of the protocol, the incumbent will need to be able to work a variable and flexible work schedule. Communication with the Sponsor is a key responsibility, as is reviewing monitoring reports and addressing the issues in the reports. Keeping the team informed of key deliverables and timelines and helping to ensure, along with the Site Director the appropriate resources. Also responsible for ongoing study drug safety reporting and follow up.
The successful candidate will have a minimum of 2 years of experience in clinical research coordination and project management experience. A degree or licensed individual is highly preferred. A demonstrated ability to drive for results by managing project teams through excellent interpersonal communication skills, motivating the group to reach a common goal and working collaboratively. Planning and organizational skills should be second nature as well as being attuned and responsive to the patient experience during the trial.
Job Type: Full-time
Experience:
- clinical research coordination and project management: 2 years (Preferred)
Education:
- Bachelor’s (Preferred)
License:
- LPN, RN, or Paramedic (Preferred)
Language:
- Spanish (Preferred)
Additional Compensation:
- Bonuses
Work Location:
- One location
Benefits:
- Health insurance
- Dental insurance
- Vision insurance
- Paid time off
This Company Describes Its Culture as:
- Outcome-oriented — results-focused with strong performance culture
- Team-oriented — cooperative and collaborative
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