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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 Discover new opportunities to grow your career as a Medical Director! Are you ready to redefine what's possible, and discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in our patient's lives. Joining our team will offer you a rewarding career, an opportunity to work in a high energy & collaborative workp
Posted 4 days ago
Job Overview Senior Clinical Research Associate Oncology USA locations and Montreal and Halifax, 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 working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee d
Posted 15 days ago
Job Overview Senior Clinical Research Associate Oncology USA locations and Montreal and Halifax, 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 working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee d
Posted 15 days ago
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing 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 (Sr ) Medical Director will play a key role in people leadership/management, client relations,
Posted 15 days ago
Job Overview Senior Clinical Research Associate Oncology USA locations and Montreal and Halifax, 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 working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee d
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 Project Manager, Oncology Home Based Anywhere in the United States or Canada Full Time Therapeutic Area Experience Required Oncology At times working under the direction of a Project Director; the Senior Project Manager oversees and manages domestic, regional and/or international projects. Responsibilities typically include developing and managing project teams, communications,
Posted 17 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 Project Manager, Oncology Home Based Anywhere in the United States or Canada Full Time Therapeutic Area Experience Required Oncology At times working under the direction of a Project Director; the Senior Project Manager oversees and manages domestic, regional and/or international projects. Responsibilities typically include developing and managing project teams, communications,
Posted 17 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
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