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 ...

The role:* Provide Support to various projects* Maintain and Tracking clinical study documentation* Coordinate study materials* Collate relevant study information. You will need:* Strong Administrative skills* Organizational skills to support several team members.* Excellent written and verbal communication* Working Knowledge ...

Pune Responsibilities 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- ...

Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Covance Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of ...

Job Description Skill required: Clinical – SDTM Programming Designation: Clinical Data Programming Associate Job Location: Bengaluru Qualifications: Any Graduation 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 ...

Skill required: Data Maintenance – Clinical Data Management Designation: Associate Job Location: Bengaluru Qualifications: Bachelor of Pharmacy/BSc/MSc 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 ...

Skill required: Clinical Data Management (CDM) – Study Build Designation: Associate Job Location: Bengaluru Qualifications: Any Graduation 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 ...

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 ...