• Close interaction and collaboration with study team lead and study team members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Speci...
...Transparency submission documents are delivered in accordance with timelines, high quality, operational and technical procedures.
May attend Transparency Submission planning meetings with cross-functional team me...
...Submission Teams (CST) to ensure compliance of documentation to internal company standards and external regulatory guidelines.
Program Writer ensuring adequate medical writing resources are available for assigned...
...we can help you build the career you want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter
Provide project and technical support in the preparation, ...
...The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with cli...
Supervise a group of nursing students in a variety of clinical training rotations, facilitating their participation in care and treatments and evaluating student performance
Communicate clearly and directly to students, clinical site staff and oth...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...training rotations, facilitating their participation in care and treatments and evaluating student performance
*Communicate clearly and directly to students, clinical site staff and other coordinating professional...
...Main Duties:
Management of one or more projects with a focus on delivery of the scope on time, within budget and with a high-quality outcome
Project Manager in their project delivery needs ...
