Precision for Medicine is looking to improve the speed, cost and success rate of bringing life-changing therapies to patients by integrating clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.
Requirements
- 3+ years of CRA experience within the CRO or pharmaceutical industry
- Experience in biopharma or relevant therapeutics areas
- Fluency in Serbian, English and Bulgarian languages
- Study start up activities experience
- Experience with Phase I studies
- Understanding of financial management
Responsibilities
- Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
- Handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.
- Train and mentor junior staff members.
- Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Other
- 4-year college degree or equivalent experience
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
- Ability to work in a remote setting
- Strong communication and conflict resolution skills
