Responsibilities Clinical Research Associate Job Description Additional Responsibilities May Include Qualifications Apply: https://www.linkedin.com/jobs/view/4090931912/?alternateChannel=search&refId=zHRVLjWiSTi1V0ty6DHOsA%3D%3D&trackingId=6BGQpa8iBkdo28AP77oplw%3D%3D

Data Validation (cleaning) Data Management Documents/Plans (Trial Master File) Study Start-Up Activities And User Acceptance Testing (UAT) Data Tracking And Entry Project Quality Management & Compliance Training Skills Knowledge And Experience Location: Hybrid Education Apply: https://www.linkedin.com/jobs/view/4128398299/?alternateChannel=search&refId=zHRVLjWiSTi1V0ty6DHOsA%3D%3D&trackingId=tfPgUIPwsS73b6FfmLI5pg%3D%3D

About The Role 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 ...

Specific requirements for this role Review of Statistical Analysis Plan for First in Human (SAD), Phase II – IV trials and review trial protocols, SAS datasets, TLF’s and Clinical Study Reports Review and ensure compliance of Pharmacometrics & Statistical processes ...

Location:  Halol 2 Job Description  To provide support for execution and monitoring of trial, scale up, exhibit process qualification batches.To prepare and review new product documents like  material requirement sheet, master formula card, bill of material, master formula, risk assessment reports ...

Responsibilities: Oversight of CRO / other vendors and study management- Perform regular reviews of data according to data review/monitoring guidelines (CTMS, EDC, IVRS etc.) Collaboration with cross functional teams- Soft skills- Qualifications: Apply: https://careers.sunpharma.com/job/Mumbai-Manager-2-Global-Trial-Manager/21152544/

Project Management Enterprise Leadership Minimum Qualification Requirements: Other Information/Additional Preferences: Apply: https://lilly.wd5.myworkdayjobs.com/en-US/LLY/details/Principal-Study-Build-Programmer_R-78336?q=clinical%20trials&source=linkedin&jobFamilyGroup=99c6e09d03e801a7d2687e7ff04aec33&locations=11eaf73f269c01454efffa5b2c4c9d27&locationCountry=c4f78be1a8f14da0ab49ce1162348a5e

BA/BE: Section Bioanalytical Laboratory operations Section activities Central laboratory section activities Clinical trials, data management, statistics, and pharmacy section activities As a Syngene leader: Education and Experience Education M. Pharm, MSc – Post graduate degree in life sciences, Minimum required. ...

The Position The Publication Project Manager is responsible for managing global publication plans, publication budgets, and collaborating closely with medical affairs colleagues, the medical writing team, affiliate offices, and external HCPs. Qualifications Apply: https://careers.novonordisk.com/job/Bangalore-Global-Publication-Project-Manager-Karn/1154417301/

Location:  Tandalja – R&D Apply: https://careers.sunpharma.com/job/Baroda-Senior-Manager-2/18377644/

Location:  Tandalja – R&D Key Responsibilities: Apply: https://careers.sunpharma.com/job/Baroda-Executive/32092044/

30% Support Outsourcing Team 25% Vendor management: 15 – 25 Vendor per study 35% Vendor selection and contract negotiation: Apply: https://careers.sunpharma.com/job/Mumbai-Senior-Manager-Clinical-Outsourcing/17749744/

Role: Associate Research Physician/Associate Manager Key Responsibilities:  Educational Qualification:  MBBS MD Pharmacology. Experience:  2-5 years Behavioral Skills: Apply: https://careers.syngeneintl.com/job/Bangalore-Medical-Monitor/1206685300/

The Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related ...

Data Validation (cleaning): Data Management Documents/Plans (Trial Master File): Study Start-Up Activities and User Acceptance Testing (UAT): Data Tracking and Entry: Project Quality Management & Compliance: Training: Skills: Data Validation (cleaning): Data Management Documents/Plans (Trial Master File): Study Start-Up Activities ...