Key Responsibilities:  1. Supporting the Clinical Project Manager for coordination with-in the project team.  2. Delegation of project level Clinical Project Manager responsibilities 3. The above responsibilities would be assigned by reporting manager and project-level task allocation would be performed. Educational Qualification:  ...

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

Job description Seeking an Experienced Clinical research Coordinator. Responsibilities include planning clinical trials, coordinating study tasks, managing essential documents, aiding IRB submissions, and ensuring regulatory compliance. EducationUG:  B.Pharma in Any SpecializationPG:  M.Pharma in Any Specialization Apply: https://www.naukri.com/job-listings-clinical-research-coordinator-spirant-communication-pvt-ltd-noida-greater-noida-delhi-ncr-3-to-6-years-070125006796?src=simjobsjd_bottom

Job description ORGANISATIONAL OVERVIEW JOB DETAILS Apply: https://www.naukri.com/job-listings-clinical-research-associate-i-lambda-therapeutic-research-limited-ahmedabad-3-to-7-years-060125507899?src=simjobsjd_rt

Key Responsibilities 1. Clinical Study Design and Execution Lead the design, planning, and implementation of clinical studies, particularly in areas requiring pharmacokinetic and pharmacology expertise. Monitor and report the studies at CRO Develop study protocols, investigator brochures, and other study-related ...

Job description Role & responsibilities:- Preferred candidate profile:- Apply: https://www.naukri.com/job-listings-clinical-nurse-cliantha-research-ahmedabad-2-to-5-years-280823000920?src=jobsearchDesk&sid=undefined&xp=17&px=1&nignbevent_src=jobsearchDeskGNB

Job description Role & responsibilities Off-site Monitoring: 1-Conduct off-site visits during different study phases, including initial site visits to train and guide site personnel.2-Ensure the site is ready for the study by inspecting pre-requisites as per the study protocol.3-Undertake routine ...

Responsibilities Qualifications Apply: https://www.linkedin.com/jobs/view/4132908107/?alternateChannel=search&refId=7g7aoEWCcQAKHMH7LR6ZZQ%3D%3D&trackingId=rva0iruAgEnQJP0I%2FqsEQw%3D%3D

Job Description Role: Senior Clinical Research Associate 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/4135506079/?alternateChannel=search&refId=ZyLHx6KCkcxrvyQ5LdNwDA%3D%3D&trackingId=M1dSfJtwPK1gK%2F7EYjUAyg%3D%3D

Qualifications Must-Have Nice-to-Have Apply: https://www.linkedin.com/jobs/view/4133850559/?alternateChannel=search&refId=GywJt0Xqlq1IWINYBvnsRQ%3D%3D&trackingId=SRXRj8NoMvJdObp%2FCJvcPQ%3D%3D

Main Responsibilities The Central CRA serves as the primary liaison for the Principal Investigator and other site staff involved in conducting rare disease registries at the investigational site. Feasibility Activities Study Start-up Activities Site Monitoring Site Management Safety & Quality ...

Primary Responsibilities : ·       Drive end-to-end process delivery and improvements in regulated and policy-driven clinical disclosures and data sharing. ·       Serve as the primary point of contact for project teams and functional matrix teams for Clinical Trial Transparency activities. ·       Assess HSR trials ...

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/

Responsibilities The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables.  This role coordinates for all services contracted for the study. CTMs are also ...

Job description Draft and edit clinical study protocols and informed consent forms.Prepare manuscripts for publication, ensuring adherence to journal formatting and structure. Mandatory criteria: Must have authored at least one original article in a medical journal. Education: PG: MS/M.Sc(Science) in Biotechnology, ...