Clinical Facilitator

Summary -Responsible to support all statistical programming data review reporting and analytics development aspects of assigned studies or project-level activities Major accountabilities 1 Produce and track reports for various line functions within Global Drug Development used for ongoing monitoring of clinical data 2 Provide understandable and actionable...

**Principal Clinical Programmer (RAVE EDC)** Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with...

Summary Job Title Clinical Sourcing Manager R D LI-Hybrid Location Hyderabad India The Clinical Sourcing Manager generates negotiates and executes contracts to support the utilisation of clinical Contract Research Organisations CROs for Novartis Clinical Trials This role assures compliant high-quality timely and cost-effective external service delivery to...

Job Title **:Clinical Trial Assistant (CTA)** Location : Hyderabad, Punjagutta Officers Colony, 702 & 801, Pavani Prestige Commercial complex, Piller no 1074, Punjagutta. Organization : Forward Life Pvt Ltd [Clinical Research Organization] Employment Type : Full-Time/ Rotational Shifts Gender : Male **Job Summary**: The Clinical Trial Assistant (CTA)...

Position: Clinic CoordinatorLocation: Habsiguda, HyderabadJob OverviewWe are seeking a Junior Level Clinic Coordinator to join our team in Hyderabad on a full-time basis. The ideal candidate will have 1 to 3 years of experience and will be responsible for efficiently managing clinic operations and ensuring a seamless experience for patients and...

Your responsibilities include, but are not limited to:•Contribute to electronic Case Report Form (eCRF) development with a thorough understanding of data to be collected and in alignment with the protocol. •Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated...

Job description Support a PI sponsored Investigational New Drug (IND) or Investigational Device Exemption (IDE) Host/ prepare for external audits (sponsor, FDA, NIH, etc) Monitor or audit studies in the institution Facilitate and/or run research/project team meetings Prepare study budget Educate and mentor clinical staff, research team and other...

Job Summary: Continental Hospitals is seeking a dedicated and experienced Clinical Research Coordinator with a minimum of 3 years of experience in clinical trials. The ideal candidate will be responsible for the coordination, management, and execution of clinical research studies in compliance with applicable regulations, protocols, and institutional...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all You ll lead with purpose breaking down barriers to innovation in a more connected compassionate world A Day in the Life Senior Clinical Evaluation medical writer PSUR creation for Surgical OU Responsibilities may include the...

Your responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...