Clinical Data Management Pharmacovigilance Jobs

Clinimed Pharma - Remote

,Pharmacovigilance,Clinical Data Management & Medical WritingB.Pharm, M. Pharm, Pharm D, MSC. (Any Life Science Stream), BE - Biotech. BDS, BAHS, BAMS 2023 freshers only. 3 Lacs PA INR

from: naukri.com - 4 days ago

Lifelancer - Bengaluru / Bangalore, India

such as: o Clinical trial coordinator at site Clinical data management Pharmacovigilance Records management Key Personal Attributes: Highly personable nature that fosters teamwork Excellent communication Not Mentioned

from: Monsterindia.com - 9 days ago

Guardians EdTech - Bengaluru / Bangalore, India

background in Clinical Research, including expertise in Pharmacovigilance, Regulatory Affairs, Clinical Data Management, and Medical Writing. The candidate should be passionate about education and possess Not Mentioned

from: Monsterindia.com - More than 30 days ago

Lifelancer - Hyderabad / Secunderabad, Telangana, India

Management, relevant experience in Pharmacovigilance relevant experience in Clinical Project Management. Please use the below link for job application and quicker response. https://lifelancer.com/jobs/view Not Mentioned

from: Monsterindia.com - 9 days ago

Ergomed - Bengaluru / Bangalore, India

specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow steps. Reconciliation activities for all types of received reports Workflow management activities Not Mentioned

from: Monsterindia.com - More than 30 days ago

Syneos Health - India

/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. For the Clinical Monitoring/Site Management Plan (CMP/SMP Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sitero - India

guidelines. Experience with safety data collection and interpretation originating from clinical trials and other sources (such as literature, solicited and post-marketing environment). Ability to build Not Mentioned

from: Monsterindia.com - More than 30 days ago

ICON plc - Chennai, India

for accuracy and quality and assist with maintaining project files. . Perform safety review of clinical and diagnostic data as part of case processing. . Responsible for effective and efficient development Not Mentioned

from: Monsterindia.com - 9 days ago

Sitero - India

with clients, management, peers and cross functional teams effectively. Good working knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines. Experience with safety data collection Not Mentioned

from: Monsterindia.com - More than 30 days ago

ProPharma - Hyderabad / Secunderabad, Telangana, India

management systems, ERPs, clinical trial, and pharmacovigilance applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Experience in authoring Not Mentioned

from: Monsterindia.com - 9 days ago