Clinical Investigator Jobs in Telangana

Dr. Reddy's Laboratories - Hyderabad, Telangana, India

• You will be responsible for supporting the strategic development of a global risk-based audit strategy and program for clinical trials. This includes performing and reporting audits of investigator sites, clinical research

from: linkedin.com - 12 days ago

Hyderabad, Telangana, India

; drive and/or contribute to the development of trial-related documents and processes Contribute, with the support of a CTL/Lead CTL and the CPL, to the development of clinical section of regulatory

from: jobleads.co.in - Yesterday

Hyderabad, Telangana, India (+1 location)

protocols, amendments 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

from: jobleads.co.in (+1 source) - Yesterday

Aizant - Ameerpet

event reports. Participant Interaction: Provide information and support to study participants regarding study medications and protocols. Cross-Functional Collaboration: Work closely with investigators 1.75-3 Lacs PA INR

from: naukri.com - 10 days ago

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 - 10 days ago

Hyderabad, Telangana, India

, amendments 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

from: jobleads.co.in - 25 days ago

Hyderabad / Secunderabad, Telangana, India

any limitation (implied or otherwise) on its ability to do so Required Qualifications: Medical degree - BHMS/BAMS/BUMS/BPT/MPT/B.Sc. Nursing Basic computer skills Attention to detail and quality focused Good Not Mentioned

from: Monsterindia.com - 13 days ago

Hyderabad / Secunderabad, Telangana, India

. Your responsibilities will include writing and reviewing a variety of documents such as clinical trial protocols, clinical study reports, investigator brochures, and informed consent forms, ensuring adherence Not Mentioned

from: Monsterindia.com - 3 days ago

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

Delhi, Hyderabad / Secunderabad, Telangana, Bengaluru / Bangalore, Chennai, Kolkata, Mumbai, Pune, India

and responsibilities may include:Assisting in Study Design: Collaborating with principal investigators (PIs) and senior researchers in designing clinical research studies, including protocol development, sample size Not Mentioned

from: Monsterindia.com - 8 days ago