Job description Role & responsibilities: Clinical Protocol Preparation Pharmacy Apply: https://www.naukri.com/job-listings-research-analyst-medical-writer-qps-bioserve-hyderabad-2-to-4-years-240125908850?src=jobsearchDesk&sid=17378828952346449_2&xp=3&px=3&nignbevent_src=jobsearchDeskGNB

Job description We believe the dedicated people who work at CBCC are the best. They each have deep compassion and a single focus on the well-being of our patients. If you would like to join our devoted team, the following ...

Position Summary: The Lead Scientist of Clinical Research will be responsible for overseeing, leading, and guiding clinical research efforts, ensuring they are carried out efficiently, in compliance with regulations, and within budget. This role involves high-level collaboration with internal teams and external ...

Clinical Team Leader will be responsible for overseeing the monitoring and site management activities on assigned clinical research projects as per business needs. REQUIRED EXPERIENCE:- Apply: https://www.linkedin.com/jobs/view/3931385660/?alternateChannel=search&refId=6al6U9exLMZFj6G04SNGxQ%3D%3D&trackingId=ubpheHsKAl2zRctoZzs1Kg%3D%3D

Qualifications Must-Have Nice-to-Have Apply: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/details/Associate-Data-Manager—Clinical-Data-Sciences_4924629-1?q=clinical%20trial&locations=e2d3979e3af101936db42457076cbe8e

Purpose/Objective of the job Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the ...

Qualifications Apply: https://www.linkedin.com/jobs/view/4131884917/?alternateChannel=search&refId=pGshJqRp71HJlG6yrxmGMQ%3D%3D&trackingId=sRCL5SZ%2BRRK3TedMZ9eqiw%3D%3D

The main responsibilities are: The job is globally oriented, and Responsibility covers clinical product development worldwide. The job requires collaboration with stakeholders within Novo Nordisk global organisation and countries all over the globe. The job is geographically placed in BLR but has global ...

The Position As a Safety Medical Writer at Novo Nordisk, you will: Qualifications We are looking for candidates with the following qualifications: Apply: https://careers.novonordisk.com/job/Bangalore-Senior-safety-medical-writer-Karn/1151759701/https://careers.novonordisk.com/job/Bangalore-Senior-safety-medical-writer-Karn/1151759701/

Key Responsibilities Educational Qualification M. Sc/M. Pharm/Pharm D, BAMS, BDS, MDS & BHMS/Any life science Experience 3 – 9 Years Behavioural Skills Apply: https://www.linkedin.com/jobs/view/4115837397/?alternateChannel=search&refId=S5W2mdvN%2B%2B%2BPqh3HmIBNYw%3D%3D&trackingId=B%2FQvRyGxBCx8IRAmlCoHlQ%3D%3D

Apply: https://careers.syngeneintl.com/job/Bangalore-QA-Auditor-Clinical/1246379300/

Job description This is a site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV Global Drug Development (GDD) trials within the country ...

Role & responsibilities : Preferred candidate profile : Apply: https://www.naukri.com/job-listings-clinical-trial-assistant-lupin-pune-0-to-3-years-301224005484?src=simjobsjd_bottom

Job description PRINCIPAL DUTIES AND RESPONSIBILITES: 1 Identify and qualify potential investigators to ensure that the sites have adequate time and can fulfill their obligation to the study. 2 To review research protocols and amendments, informed consent documents, case report form and/or ...

Core Purpose of the Role: Role Accountabilities Apply: https://careers.syngeneintl.com/job/Bangalore-QA-Auditor-Bioanalytical/1255167300/