PSUR Report Authoring and Quality Review

5 - 6 years

2 - 6 Lacs

Hyderabad

Posted:2 months ago| Platform: Naukri logo

Apply Now

Skills Required

Data management Analytical Life sciences Pharmacovigilance Subject Matter Expert Subject matter expertise Risk management Drug safety Process management Data extraction

Work Mode

Work from Office

Job Type

Full Time

Job Description

Authoring and Reviewing PSURs: Prepare and review Periodic Safety Update Reports (PSURs/PBRERs) for submission to health authorities. Ensure the accuracy, completeness, and regulatory compliance of all PSURs. Literature Search and Validation: Perform literature searches to gather relevant data for PSUR preparation. Validate the information obtained from literature searches to ensure accuracy. Data Management: Extract and validate data from various sources, including Reference Safety Information (RSI), sales data, previous reports, and Risk Management Plans (RMP). Generate Line Listings (LL) from the safety database for inclusion in PSURs. Process Management: Manage and reconcile relevant process trackers to ensure all activities are documented and on schedule. Provide reliable support for high-priority ad-hoc activities related to PSUR preparation. Client Interaction: Communicate with client personnel to resolve issues related to PSURs, ensuring adherence to client policies. Ensure that PSUR deliverables comply with regulatory requirements and are submitted within agreed timelines. Subject Matter Expertise and Training: Serve as a subject matter expert (SME) for PSUR preparation and review. Provide training and mentoring to team members on PSUR-related processes and regulatory requirements. Qualifications: Bachelors degree in a relevant scientific or medical field (e.g., Pharmacology, Medicine, Life Sciences). Advanced degree preferred. Experience in pharmacovigilance, drug safety, or related field, with a focus on PSUR preparation and review. Knowledge of regulatory requirements for PSURs/PBRERs. Strong analytical and problem-solving skills with the ability to evaluate and interpret complex safety data. Excellent written and verbal communication skills. Proficiency in safety databases and data extraction/validation processes. Strong organizational skills with the ability to manage multiple tasks and projects simultaneously. Demonstrated ability to collaborate effectively with cross-functional teams and provide expert

Mock Interview

Practice Video Interview with JobPe AI

Start Data Management Interview Now
Vizen Life Sciences
Vizen Life Sciences

Biotechnology

San Francisco

50-100 Employees

11 Jobs

    Key People

  • Dr. Alice Johnson

    CEO
  • Mark Smith

    CTO

RecommendedJobs for You