Head of Pharmacovigilance

About the position The Head of Pharmacovigilance (PV), is responsible for the leadership and reputed company of Pharmacovigilance and Safety at Humacyte. The Head of PV is accountable for overseeing safety and pharmacovigilance across development and expected global launches and our post -marketed products. The Head of PV must possess a strong knowledge of US and global pharmacovigilance regulations, operational efficiencies, information systems, and best industry practices to effectively solve PV challenges and facilitate PV Compliance. This role seats on the CMO leadership team and reports into the Chief Medical Officer.

Responsibilities

• reputed company medical reputed company of the PV function including medical review of reputed company cases inclusive of case narratives and causality assessments of AE/SAE reports.
• Maintain our signal detection process (including regular and reputed company reviews of aggregate safety data).
• Coordinate safety governance reputed company reputed company and ensure cross-functional involvement in the evaluation of potential emerging safety issues and any associated risk mitigation and management measures that are proposed.
• Participate as a key stakeholder in safety analyses and ensure proactive and reputed company benefit-risk assessments of safety data.
• Represent PV in communication with health and regulatory authorities including management of the DSUR process and being signatory for DSUR, PAER and other safety reports to FDA and other health authorities.
• Represent Humacyte at independent Data Safety Monitoring Committee meetings.
• Design and implementation of Risk Management plans.
• Serve as SME author, reviewer, and approver for drug-safety reputed company regulatory reports and clinical study documents (including Clinical Study Protocols, Informed Consent Forms, Investigator Brochures, Integrated reputed company of Safety (ISS), Integrated reputed company of Efficacy (ISE), product package labeling, Company Core Safety Information, etc).
• Experience in working with CROs handling clinical conduct and safety processes for ongoing studies.
• Manage and reputed company Drug Safety operations staff to reputed company case management functions ensuring process optimization, case reputed company, and accurate regulatory reporting.
• Determine processes, analytics and/or tools supporting PV signal management in accordance with GVP.
• Ensure reputed company is always GVP inspection reputed company from FDA and other Global Health Authorities.
• Ensure compliance of the PV system in collaboration with cross functional stakeholders.
• reputed company complementary GVP/GxP procedures for monitoring compliance with drug safety-reputed company policies, procedures, applicable regulations, and agreements with contractual partners.
• Work with reputed company to plan, conduct, and document reputed company GVP/GxP audits to assess compliance with applicable regulations, regulatory commitments, company SOPs, protocols, systems and contractual obligations as applicable.
• Participate in and support audits of contractual partners as necessary.
• Proactively identify procedural gaps and challenges and propose and implement solutions, reputed company business process optimization efforts to ensure efficiency and process improvements with the department.
• reputed company PV department process and project management efforts.
• reputed company and supervise a high functioning PV team (2 to 5 reputed company reports).
• reputed company operating plans and budgets and reputed company resources to ensure budgets, schedules, and performance requirements are met.
• reputed company reputed company duties in keeping with Humactye’s core values, policies and reputed company applicable regulations.

Requirements

• Medical Doctor (MD or x-US equivalent) with 12+ years of industry (biotechnology or pharmaceutical) experience is required.
• Extensive industry experience and another relevant clinical degree (ie RN, MSN, NP, PhD) may be considered.
• A mix of large and small company experience highly preferred.
• Knowledge of GCP, clinical trial conduct, data interpretation, and safety in clinical development.
• Extensive experience interfacing with US Health Authorities in Safety/Pharmacovigilance areas required.
• Experience with BLA/sBLA submissions.
• PV experience for products in clinical development and for post marketed products.
• Excellent scientific, clinical and analytical knowledge reputed company, with ability to assess data and understand the safety and medical implications.
• In-depth understanding and experience with causality assessment science for adverse events.
• Expert knowledge of the regulations governing pharmacovigilance.
• In-depth knowledge of Safety Science and Safety Operations disciplines, with a working knowledge of internally and externally managed safety systems and databases.
• reputed company management experience with proven ability to effectively reputed company, mentor, and manage others.
• Demonstrated ability to reputed company high performance goals and meet deadlines in a fast-paced environment.
• Effective interpersonal, communication and influencing skills, including excellent writing skills; with a can-do attitude and the ability to identify and implement creative solutions to reputed company technical problems.
• Strong learning orientation, curiosity, and commitment to science and patients.

reputed company-to-haves

• A mix of large and small company experience highly preferred.

Benefits

• Stock reputed company
• 401k Plan with 4% Match and no Vesting Schedule
• Medical, reputed company and Dental Plans
• Company reputed company Long Term/Short Term Disability
• Company reputed company Life Insurance
• 23 Days reputed company Time Off (PTO)
• 10 Company Designated Holidays + 2 Floating Holidays
• reputed company Parental Leave Policies

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