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Job Overview Reporting to the Vice President, the primary role of the incumbent will be to provide subject matter and drug development expertise in support of clinical drug development trials in rare diseases as well as pediatric patient populations. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Medical Director or Sr.
Posted Today
Job Overview CRA I or II, Oncology Experience Required Why settle for one thing when you can have everything. Covance gives you the best two for one opportunity for career growth. Who doesn't want twice the perks working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee dedicated to an FSP project you will bring your sp
Posted Today
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to provide subject matter and drug development expertise in support of Respiratory/Pulmonary, Critical Care, and Infectious Disease drug development trials. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Medical Director o
Posted Today
Job Overview Senior Clinical Research Associate Why settle for one thing when you can have everything. Covance gives you the best two for one opportunity for career growth. Who doesn't want twice the perks working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee dedicated to an FSP project you will bring your specializ
Posted Today
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or ot
Posted 7 days ago
Job Overview CRA Drug Accountability (Unblinded CRA) Covance is seeking an Unblinded CRA to cover the Western Region of the US. This is a specialized CRA role which primarily focuses on drug accountability at a site level across a range of protocols and therapeutic areas. Essential Job Duties Responsible for all aspects of study site monitoring including routine monitoring and close out of clinica
Posted 10 days ago
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or ot
Posted 15 days ago
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or ot
Posted 17 days ago
Job Overview Senior Clinical Research Associate Why settle for one thing when you can have everything. Covance gives you the best two for one opportunity for career growth. Who doesn't want twice the perks working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee dedicated to an FSP project you will bring your specializ
Posted 27 days ago
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