• 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...
...and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
The Regualtory Specialist I prepares and maintains complete and accurate regulatory documents in su...
...Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retire...
...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...
...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...
...Tabulation Mode deliverables.
Active participation in sharing better practices on use of standards in alignment with Lead Clinical Data Programmer and Process & Automation Specialist.
Maintain system related d...
TCS is hiring for Study Delivery Specialist!Role: Study Delivery Specialist(SDS)Work location: Mumbai/Pune/BangaloreExperience: 5 8 years’ relevant experience in Study Delivery SpecialistQualification: Any life science GraduateJob Description:SDS is ...
...members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Specification Worksheet (SSW) to facilitate ...
