136 to 150 of 502
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 4 days 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 4 days ago
Supervises the day to day production and non production activities of the local departmental employees. Directly monitors the quality of testing services provided by employees under his/her supervision. Assigns appropriately trained personnel and ensures sufficient number of staff are available to complete the workload. Supervision Schedules department personnel appropriately to match the demands
Posted 4 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 4 days 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 4 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 4 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 4 days 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 4 days 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 4 days 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 4 days 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 4 days 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 4 days 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 4 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 4 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 4 days ago
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