Required CRA1 - Hematology /Rheumatology Experience- CFSP - Israel
Your responsibilities will include:
Performing site selection, initiation, monitoring and close-out visits after completing training period
Supporting the development of a subject recruitment plan
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
Collaborating with experts at study sites and with client representatives
What you can expect:
Resources that promote your career growth
Leaders that support flexible work schedules
Programs to help you build your therapeutic knowledge
Excellent working environment in a stabile, international, reputable company
Mobile phone and attractive benefits package.
Requirements: University degree in scientific discipline or health care
At least 6 moths of experience in Pharma Industry, and/or Clinical Trials environment
Very good computer skills including MS Office
Excellent command of Hebrew and English language
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Drivers license class B.
This position is open to all candidates.