Sr. Director Pharmacovigilance Compliance - Madrigal Pharmaceuticals Corporation
Conshohocken, PA 19428
About the Job
Position Responsibilities:
- Develop, maintain and track process for monitoring compliance of Madrigal PV System including regulatory compliance pertaining to PV requirements
- Compile, analyze, and trend pharmacovigilance compliance data including root cause assessments, gap analysis and effectiveness of improvement plans
- Provide monthly compliance reports to Sr. Management including associated mitigation strategies. Provide report to Qualified Person(s) for PV as required
- Identify need and create PV CAPA for non-compliance. Collaborate with relevant team members to implement and track until closure
- Ensure necessary procedural documents are in place to enable a compliant PV System including identification of process enhancements/continuous improvement
- Collaborate PV MD, VP, PV Safety and Compliance and other team members, as required, to develop and implement a strategy for compliance trending and reporting on ICSR and aggregate safety reports quality and submission timelines; signal management tracking and timelines; and RMP submission and commitment timelines
- Assume responsibility for ensuring regulatory intelligence process and management is in place. Evaluate and conduct impact assessment for legislative/regulatory changes affecting PV
- Provide necessary PV quality and compliance information for inclusion in PSMF
- Act as primary PV contact for inspections and audits
- Collaborate with PV person(s) responsible for vendor oversight to define KPIs reflective of business practices. Implement, measure and monitor compliance
- Perform QC of PV documentation to be used for external submissions such as PV aggregate reports, PSMF, RMP etc.
- Ensure a state of Inspection Readiness including necessary training for all relevant Madrigal employees and vendors, as required
- Bachelor's degree in healthcare/scientific related field with minimum of 8 years of relevant experience in PV with a minimum of 4 years in PV compliance and quality
- A proven track record in pharmacovigilance with several examples of supporting pharmacovigilance compliance monitoring and quality activities
- Solid experience being PV lead for inspections and audits
- Expert knowledge of regulatory requirements pertaining to FDA, EU Good Pharmacovigilance Practices, and pharmaceutical industry compliance practices, which includes solid knowledge of safety reporting in clinical trials, post marketing surveillance, case processing and reporting to global Regulatory Authorities, in particular US, EU and UK.
- Solid experience in quality systems, safety systems and compliance monitoring
- Direct experience and knowledge of case processing/ case management, data quality review for aggregate reports and RMPs and evaluation/reporting of PV system performance is required
- Direct experience with creating, tracking, compiling, and analyzing quality metrics is must
- Demonstrated ability to apply principles, concepts and industry best practices governing pharmacovigilance in assigned projects and company deliverables
- Highly organized, outcome oriented, problem solving, understanding of research methods and basic data analysis
- Demonstrated ability to work independently as well as collaboratively with other team members
- Excellent written and verbal communication skills; must be able to communicate effectively regarding safety data, and issues related to safety and pharmacovigilance
Compensation:
Base salary is determined by several factors that include, but are not limited to, a successful candidate's qualifications, skills, education, experience, business needs, and market demands. The role may also be eligible for bonus, equity, and comprehensive benefits, which include flexible paid time off (PTO), medical, dental, vision, and life and disability insurance.
Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law.
Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established.
Please be aware that we are currently receiving numerous reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals’ Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal’s name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Interviews with Madrigal are conducted via the Zoom platform.
Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for Madrigal we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks.
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