Job responsibilities•    Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.  Uses judgment and experience to evaluate overall performance of site ...

Duties and Responsibilities: Learns to draft protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information. Learns to communicate and interact with study team, other departments and clients as applicable. Learns to plan, ...

Job responsibilities •    Review of the central LNR database to assess the availability of the local laboratories being used on a project. Communicate with the project team to obtain LNRs not available in the central LNR database. •    Transcription of the raw ...

Essential Duties and Responsibilities: As Quality Check Reviewer Review data entered in safety database for completeness and accuracy. Provide quality feedback to team resources Track and maintain quality metricsAs Case Processor Responsible for data entry of Individual case safety reports ...

Overview 1. Reviewing the published reports/biomedical literature to ascertain if they contain individual case reports and Non-individual case reports.2. Applying regulatory and internal guidance to determine if the article meets the definition of a valid case report and Non- individual ...

Job Description Skill required: Pharmacovigilance – Medical Affairs Designation: Associate Job Location: Bengaluru Qualifications: Bachelor of Pharmacy Years of Experience: 1-3 years Roles and Responsibilities In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected ...

As a Data Scientist I you will be responsible for developing business requirements with project managers and analytic leads and other clinical staff to create industry decision support solutions, including clinical trial tokenization (CTT) analytics, that are used in the course of ...

Actively Hiring Freshers / Junior resources in Chennai: “Associate Record Management Specialist” with experience in eTMF, VEEVA and eCTD.Experience required: 0-2 years (freshers having Clinical Research Courses with knowledge on eTMF, VEEVA and eCTD may apply). Interested: Kindly share updated ...

Responsible for project management support to the Scientific Writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases Initiate submission (as required), amend submission based on comments (as required) Support the Writer with the ...

Job responsibilities •    Review of the central LNR database to assess the availability of the local laboratories being used on a project. Communicate with the project team to obtain LNRs not available in the central LNR database. •    Transcription of the raw ...

About the job Job Description: Role: Clinical Research Associate (In-house CRA) Location: Bangalore/Mumbai Work Experience:3-6 Years RESPONSIBILITIES • Perform deliverables in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. ...

Experience: 0.00 – 1.00 yearsPosition Type: NAFunctional Area: Old – Medical WritingEducation: M.PharmWork Location: Bangalore Job Summary: A Trainee Scientific Writing needs to write, edit, reconcile, and manage high-quality medical and scientific communications, including abstracts, literature slide sets, and manuscripts, using data from various sources ...

Walk in Interview for freshers on 11th June 2022 Walk in interview for Freshers aragen Open Positions: Junior research associate Qualification: MSc (Organic/ General/ Integrated Chemistry) Work Location: Hyderabad Interview Location: Survey No. 125 & 126, IDA Mallapur, Hyderabad 500 ...