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Develop Data Transfer Agreement and Data Transfer Specifications for vendor data transfers. Create Edit checks for all external data types and perform validation. Review data discrepancies generated by study specific edit checks for External data and perform the subsequent query management process in resolving the data issues. Perform review of the electronically transmitted data for a sample of t
Posted 5 days ago
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing medical delivery services and subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Senior Medical Director will play a key role in people leadershi
Posted 10 days ago
Job Overview Reporting to the Executive Medical Director and/or Sr. Medical Director, the primary role of the incumbent will be to serve as a physician providing medical delivery services and subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Associate Medical Director will play
Posted 17 days ago
Job Overview Unblinded CRA Must be located in the West Region of the USA Covance is seeking an Unblinded CRA to primarily focus 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 clinical sites, maintenance of study files, conduct of pre stu
Posted 18 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 20 days ago
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing medical delivery services and subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Senior Medical Director will play a key role in people leadershi
Posted 21 days ago
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 21 days ago
This role requires an individual possessing strong professional leadership and management capabilities deemed necessary to lead a large scale medical and therapeutic led organization. Additionally, he/she will manage across a complex global organization and deliver exceptional client performance and high caliber CRO/pharmaceutical services. The ideal candidate will have a proven track record as an
Posted 24 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 27 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 1 month 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 1 month ago
to include; Client Relationship & Business Development Activities Partnering with GCO to develop new and enhance existing client relationships where possible Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team Leverage known and builds new relationships with investigators/sites to performs site/ investigator feasibility and to support op
Posted 1 month ago
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 1 month ago
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