The Safety Risk Lead (SRL) will perform proactive Safety Surveillance (SS) and Risk Management with focus on signal detection and evaluation, risk assessment and safety risk minimization. ROLE RESPONSIBILITIES
- Act as a Point of Contact for Safety in the Asset Teams, ensuring a unified communication on safety matters and representing WWS position(s) on safety
- Provides disease area specific pharmacovigilance expertise, and applies this to various business unit products assigned to the SRL operating from a SSRM DA-Cluster. Each SSRM DA-Cluster functions as a "Centre of Excellence"
- Ensures consistency of Safety Risk Messaging for a particular product or class of products, across multiple indications/BUs within the many safety reports and communications for that product. Providing suitable summaries of product risks to summary document authors where appropriate, for example providing medical content/B-R statements and overall risk messaging of the safety profile to WSR/SER Authors
- Performs ad hoc special scholarly Safety Surveillance & Risk Management activities, rapidly, to meet specific needs in the BUs, such as RRT deliverables/emerging safety issue white papers/product Due Diligence Assessments
- Identifies opportunities for Consistency and Standards for Safety Surveillance & Risk Management approaches and processes within a DA-Cluster and across BUs, and supporting the piloting and implementation of such
- Innovates, champions and implements novel approaches to Safety Surveillance & Risk Management across BUs: engages in Continuous Improvement initiatives, Safety Sciences Research & Communications activities, including methodological improvements
- Engages in inspection readiness and support. Provision of data to project managers for metrics and activity tracking.
- Fully independently evaluates complex safety data of any source, identifies and independently analyzes complex safety signals, and presents medical evaluation of safety signals and complex benefit-risk assessments to the appropriate forums
- Contributes SSRM perspective and advanced subject matter expertise to all relevant areas of risk management plans, expert reviews, Health Authority queries and other documents as required
- Prepares advanced/complex action plans to address risk and benefit-risk issues, often requiring cross-functional activity to address safety issues, including complex Risk Management activities
- Conducts and Represents SSRM on complex due diligence activities. Coaches others in due diligences
- Provides guidance and/or oversight to any team member on safety issues. Provides formal and informal education to other SSRM and team colleagues on key safety and pharmacovigilance topics. Coach others in PV/RM.
- Represents WWS on safety and benefit-risk issues to external groups including regulatory authorities and business partners
- Contributes to intra- and interdepartmental policies and procedures and plans for the implementation of new policies and procedures
- Independently initiates, conducts and chairs RMC, P-BRC (chair) and CWGs
- Prepares and contributes to written complex safety assessments and advanced benefit-risk evaluations.
- Reviews safety assessments/evaluations/contributions prepared by other SRLs and safety other colleagues.
- Independently prioritizes and completes all activities including multiple complex activities
- Makes decisions based on clinical experience.
- Utilizes knowledge of integrated body systems' pathophysiology to evaluate the impact of product issues
- Assesses the suitability of biopharmaceutical products on typical physician practice within various health systems, hospital and non-hospital patient care facilities
- Ensures products fulfil quality medical care
- For early development programs serve as a safety consultant to Clinical
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
- Education: MD (physician) degree required
- Minimum 7 years of: medical (e.g. patient care, clinical trial experience/investigator, academic medicine, specialty training and/or board certification), and/ or scientific, and/or pharmacovigilance or and/or drug development experience required
- Oncology Disease Area specific knowledge is preferred, including understanding of Oncology drug development
- Thorough understanding of Safety Risk Management internal and external environment, including applicable regulations and guidances
- Clinical development and post-marketing experience to have an understanding of safety context across the drug lifecycle
- Demonstrated leadership in day-to- day activities and collaborative skills
- Demonstrated self-awareness and interpersonal skills for successful execution of the role
- Demonstrated ability to handle more than one complex project simultaneously, prioritizing well and recognizing key issues
- Ability in, and track record of, working effectively in an advanced matrix structure, including matrix team leadership/representation preferred
- Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization
- Relevant knowledge of Pharmaceutical Company organizational structure, policies, and practices, as applicable to safety Risk Management
Technical Skills, (plus knowledge, experience and ability in):
- Safety data review, Safety data assessment, Clinical Safety signal identification, risk identification and risk management. Understands aggregate safety data and signal assessment, and performs benefit-risk assessments. From a medical perspective, independently evaluates safety data, identifies and independently analyzes safety signals, and presents the medical evaluation of safety signals to the appropriate forums
- Matrix safety team leadership
- Understanding of the scientific basis for therapies and drug-induced diseases. Effective interactions with key external subject matter experts including regulatory authorities
Other Job Details:
- Disease Area specific knowledge is preferred (Anti-Infectives; Internal Medicine)
- Thorough understanding of Safety Risk Management internal and external environment, including applicable regulations and guidances.
- Clinical development and post-marketing experience to have an understanding of safety context across the drug lifecycle.
- Relevant knowledge of Pharmaceutical Company organizational structure, policies, and practices, as applicable to safety Risk Management.
Last Date to Apply for Job: February 15th, 2022
Additional Location Information: New York, NY; Collegeville, PA; Groton, CT; Peapack, NJ; UK - Walton Oaks; UK - Sandwich
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