What are the responsibilities and job description for the Clinical Science Program Specialist position at Dawar Consulting?
Job Description
Our client, a leading diagnostics and life sciences client, is looking for Clinical Science Program Specialist .
Job Title : Clinical Science Program Specialist
Job Duration : Long Term Contract (Possibility Of Extension)
Job Location : Tucson, AZ
Our client provides integrated solutions for diagnostic testing in commercial and hospital labs, medical centers and laboratory networks. Our products and solutions support health care professionals in clinical decision making in a wide field of indications including, cardiovascular, infectious diseases, metabolism, and oncology. We are looking for a candidate to join the department Clinical Development and Medical Affairs (CDMA).
Responsibilities :
- Work with other Clinical Development Leaders, Clinical Operations, Regulatory, Quality, Labelling, Lifecycle teams, and R&D to generate Scientific Validity Assessments and Clinical Performance plans and reports according to the IVD-Regulation for both conformity assessment and post-market follow up.
- Support Indication Area Leaders and Clinical Development Leaders in the assessment and definition of Intended Uses (IU), clinical testing purposes of the IVD products, and CDMA deliverables according to the IVD-Regulation .
- Assess clinical evidence and state of the art in medicine related to the IVD products to assess and demonstrate clinical benefit and safety.
- Work and align with Post-Market Surveillance & Vigilance (Global Regulatory & Quality) on post market obligations.
Qualifications :
Company Benefits : Medical, Dental, Vision, Paid Sick leave, 401K
If interested, please share your updated resume at hr@dawarconsulting.com / akansha@dawarconsulting.com
