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Science Jobs in South San Francisco, CA

Sr. Pharmacovigilance (PV) Clinical Scientist

Talent Software Services, Inc.

South San Francisco, CA

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JOB DETAILS
SALARY
$45–$65 Per Hour
SKILLS
Adverse Events, Biotech and Pharmaceutical, Clinical Assessment, Clinical Medicine, Clinical Research, Coaching, Data Analysis, Data Entry, Data Processing, Detail Oriented, Due Diligence, Establish Priorities, Government, Healthcare, Identify Issues, International Business, Maintain Compliance, Medical Products, Medical Records, Medical and Scientific Writing, Patient Safety, People Management, Pharmacovigilance, Presentation/Verbal Skills, Problem Solving Skills, Process Improvement, Project/Program Management, Reconciliation, Registered Nurse (RN), Regulations, Risk Analysis, Safety/Work Safety, Sales Management, Standard Operating Procedures (SOP), Tactical Operations, Time Management, Trend Analysis, Vendor/Supplier Evaluation, Willing to Travel
LOCATION
South San Francisco, CA
POSTED
3 days ago
Working Model: Hybrid, South San Francsico, CA
Working Days: Monday through Friday
Working Hours: 8 AM to 4:30 PM PT
Interview Format: Two Rounds (1. Hiring Manager [30 minutes]; 2. Upper Management [30 minutes])
Summary of Position:
The US Patient Safety Sr. PV Clinical Scientist - Pharmacovigilance (PV) Compliance Team performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Patient Safety. The Sr. PV Clinical Scientist leads clinical review of US Government Client cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities. All responsibilities are performed under the direction of the US Patient Safety PV Clinical Management. Contributes in depth knowledge of Individual Case Safety Reports (ICSRs) case processing. Has developed a variety of skills typically gained through years of professional experience. Works autonomously with minimal supervision. May lead or contribute with skills to projects. May act as coach for colleagues with less experience and provide guidance.
Key Accountabilities:
Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and ***/Roche Standard Operating Procedures (SOPs) Reviews, evaluates, and verifies potential AE information during triage to determine required action per internal policies and procedures and perform data entry of adverse events by timely completion of the case via Roche global safety database. Performs seriousness / validity/causality and conducts quality review of all cases (as applicable) based on their medical assessment
Performs labeling assessment for AE(s) received using clinical knowledge and conducted follow up for all reported cases (as applicable)
Responsible for leading efforts to ensure quality of Individual Case Safety Reports (ICSRs) is at par with company standards
Responsible for maintaining thorough knowledge of ICSR requirements for assigned Therapeutic Areas (TA)
Performs trend analysis of vendor case processing issues for assigned TA and escalates to vendor, TA Leads and US Government Client management as applicable
Update and create SOPs; lead process improvement initiatives
Responsible for developing executive summary on the quality trends observed on a quarterly basis
Ensures quality of Health Authority (HA) submissions is at par with local regulations
Responsible for Clinical Review of cases processed in-house and by vendors
Understands case processing data to evaluate error rates and potential compliance impact
Responsible for training internal US Government Client and/or vendors staff or team and ensure PV compliance
Collaborate with departments and partners on drug safety data exchange
Responsible for ensuring appropriate data correction in the safety database for identified issues or errors
Responsible for maintaining follow-up templates, ensuring successful transmission of all follow-up attempts performed by PV Compliance Team Scientist /Vendor staff via the correspondence module
Accountable for training internal and external staff members on using correspondence module Performs reconciliation of outgoing communications
Maintains robust knowledge of Technical Product Complaints (TPC) & Medical Product Complaint (MPC) for all company
products including combination products
Responsible for ensuring all product complaints are reported to the appropriate stakeholders within defined timelines
Ensures appropriate due diligence to obtain missing and/or additional information for Adverse Events (AEs) is performed in accordance with company SOPs / local and global regulations
Escalates any issues pertaining to follow up activities and provide strategic resolution to US Government Client management
Assists US Government Client management in maintaining oversight for GVP vendors
Identifies the risks and gaps pertaining to case processing for GVP Vendors
Continuously monitors feedback to inform quality improvements and updates
Responsible for performing impact assessment for any new / updated company SOPs or Health Authority requirements pertaining to ICSR processing and implements any process changes required based on the identified impact
Responsible for identifying and developing training documents (i.e., SOPs) for the targeted audience (as needed)
Assists in AE reconciliation activities and/or Case Transmission Verification (CTV) (as applicable)
Acts as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps, and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety PV Clinical management
Responsible for the preparation and development of Patient Safety presentations and participates in the education offer internal /external stakeholders/vendors as applicable
Acts as Subject Matter Expert (SME) for safety-related activities within Global Safety Database per ***/Roche SOPs
Provide support during audits and inspections
Collaborates with other patient safety teams as needed
Competencies Identified for Success:
Demonstrates capability to comprehend medical information
Demonstrates ownership, initiative and accountability
Sound decision-making abilities as demonstrated by systematic gathering of information, appropriately assessing the complexity of issues, and prioritization of tasks in a timely manner within the scope of responsibility
Demonstrates strong, dynamic leadership skills
Works well independent or within teams and is effective in collaborating with others internally and externally Ability to exercise independent judgment and discretion in matters of significance
Ability to work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
Communication and presentation skills; highly effective at summarizing and presenting key considerations and decision-points
Ability to flex and thrive in an agile and fast-changing environment
Strong attention-to-detail
Strong attention-to-detail in establishing priorities and meeting deadlines
Strong project management skills
Ability to travel domestically and internationally as per business needs
Education, Experience, and Other Requirements:
Health Care Professional degree (e.g., RN/BSN/MSN, NP, RPh/B Pharm/Pharm D, or MD)
(Required)
Minimum 5 - 7 years of experience in a biopharma company with Pharmacovigilance
responsibilities (Preferred); OR equivalent clinical experience with thorough understanding
of FDA safety regulations, ICH guidelines, and other applicable regulatory guidance
documents, global PV regulatory environment, EMA regulations (Required)
Writing experience; science/medical writing (Required)
Computer proficiency and Data entry experience (Required)
Project Management (Required)

About the Company

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Talent Software Services, Inc.

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