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Covance
- San Francisco, CA / Philadelphia, PA / Pittsburgh, PA / 17 more...
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 Today
Covance
- San Francisco, CA / Philadelphia, PA / Pittsburgh, PA / 17 more...
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 Today
Covance
- Indianapolis, IN / Chicago, IL / New Orleans, LA / 3 more...
Job Overview Unblinded 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 specia
Posted Today
Covance
- Indianapolis, IN / Durham, NC / Kansas City, MO / 5 more...
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
Covance
- Indianapolis, IN / Philadelphia, PA / San Francisco, CA / 25 more...
Job Overview Senior Clinical Research Associate Oncology, Cardiology and Rare Disease 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
Posted Today
Covance
- Indianapolis, IN / Durham, NC / Chicago, IL / 1 more...
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 Today
Covance
- Madison, WI / Indianapolis, IN / Chicago, IL / 9 more...
Job Overview 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 specialized disc
Posted Today
Covance
- Madison, WI / Indianapolis, IN / Philadelphia, PA / 14 more...
include Regulatory oversight of direct reports by ensuring regulatory training is executed,understood and implemented; Provide input to relevant SOPs and standard plans/templates when applicable Ensures training record compliance with training matrix and ensures training records are up to date; assist with coordination and implementation of on boarding of new direct reports ensuring GCP training b
Posted Today
Covance
- Princeton, NJ / Madison, WI / Austin, TX / 5 more...
1. Ensures electronic vendor data contains all protocol specified parameters, is in correct format, and data populates to the specified fields and patients correctly. 2. Develop the Data Transfer Agreement and Data Transfer Specifications for vendor data transfers. 3. Review data discrepancies generated by study specific edit checks for External data and perform the subsequent query management pro
Posted 1 day ago
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