Clinical Investigator Jobs in Secunderabad

Hyderabad, Telangana, India

to relevant cross-functional stakeholders. Contribute to the development, review, and approval of clinical study documents including but not limited to informed consent forms (ICF), investigator’s brochure (IB

from: jobleads.co.in - 15 days ago

Novartis India - Hyderabad, Telangana, India (+1 location)

and related documents; drive and/or supprt trial-related documents and processes. development of clinical section of regulatory documents like Investigator’s Brochure, safety updates, IND/NDA submission

from: jobleads.co.in (+1 source) - 29 days ago

Optum - Hyderabad

Attention to detail and quality focused . Good analytical and comprehension skills . . Health Insurance knowledge,managed care experience . Claims processing experience . . Not disclosed INR

from: naukri.com - 6 days ago

Dr Reddys - Hyderabad / Secunderabad, Telangana, India

and ensure sites are compliant with project specific training requirements. 5) Ensure adequate oversight to clinical trial by Investigator throughout. 6) Address and resolve issues at sites, including the need Not Mentioned

from: Monsterindia.com - More than 30 days ago

Lifelancer - Hyderabad / Secunderabad, Telangana, India

), and regulatory requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators. Clinical Trial Monitoring: Perform routine monitoring visits to assess site Not Mentioned

from: Monsterindia.com - 21 days ago

The George Institute For Global Health - Hyderabad / Secunderabad, Telangana, India

Study Design: The Clinical Research Associate would be expected to: Assist with the identification and selection of investigators to undertake the study Conduct feasibility assessment Assist Not Mentioned

from: Monsterindia.com - More than 30 days ago

Bristol Myers Squibb - Hyderabad / Secunderabad, Telangana, India

would not be considered. Key Responsibilities Authors complex clinical documents [eg, Investigator's Brochures (IB), Protocols, Phase 2/3 Clinical Study Reports (CSR), briefing documents, Common Technical Document (module Not Mentioned

from: Monsterindia.com - More than 30 days ago

Novartis India - Hyderabad / Secunderabad, Telangana, India

/program, in collaboration with cross-functional teams.` Responsible for investigators meeting organization and all internal meetings related to the clinical study execution and operational excellence Not Mentioned

from: Monsterindia.com - 21 days ago

Novartis India - Hyderabad / Secunderabad, Telangana, India

procedures. Might be required to lead other projects/program, in collaboration with cross-functional teams. Accountable for investigators meeting organization and all internal meetings related to the clinical Not Mentioned

from: Monsterindia.com - More than 30 days ago

Novartis - Hyderabad / Secunderabad, Telangana, India

and processes. development of clinical section of regulatory documents like Investigator s Brochure, safety updates, IND/NDA submission documents, responses to Health Authorities questions. support the global Not Mentioned

from: Monsterindia.com - More than 30 days ago