136 to 150 of 501
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 day 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 day ago
Proactive follow up with Sponsor and Third Party Vendor to ensure comprehensive understanding of study design and technology design with a view of providing quality deliverables. Active participation in study team meetings. Review and provide input on requirements and specifications. Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completio
Posted 1 day 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 day 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 day 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 day ago
Job Overview Who we are Covance is now part of LabCorp. LabCorp, an S&P 500 company, is a leading global life sciences company that is deeply integrated in guiding patient care, providing comprehensive clinical laboratory and end to end drug development services. With a mission to improve health and improve lives, LabCorp delivers world class diagnostic solutions, brings innovative medicines to pa
Posted 1 day ago
Proactive follow up with Sponsor and Third Party Vendor to ensure comprehensive understanding of study design and technology design with a view of providing quality deliverables. Active participation in study team meetings. Review and provide input on requirements and specifications. Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completio
Posted 1 day ago
Job Overview Senior Clinical Scientist Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada 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 ? W orking at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeut
Posted 1 day ago
Job Overview Senior Clinical Scientist Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada 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 ? W orking at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeut
Posted 1 day ago
Proactive follow up with Sponsor and Third Party Vendor to ensure comprehensive understanding of study design and technology design with a view of providing quality deliverables. Active participation in study team meetings. Review and provide input on requirements and specifications. Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completio
Posted 1 day ago
Proactive follow up with Sponsor and Third Party Vendor to ensure comprehensive understanding of study design and technology design with a view of providing quality deliverables. Active participation in study team meetings. Review and provide input on requirements and specifications. Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completio
Posted 1 day ago
Job Overview Senior Clinical Scientist Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada 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 ? W orking at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeut
Posted 1 day ago
Job Overview The Team Supervisor is responsible for the day to day coordination and supervision of the department to ensure the successful implementation of the Laboratory Pre Analytical Services strategy, structures, processes, and metrics in order to deliver outstanding customer satisfaction. This role will start on the first shift which is Tuesday Saturday (5am 2pm) and after several months mov
Posted 1 day 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 day ago
Email this Job to Yourself or a Friend
Indicates required fields