Manager, GCP Quality Assurance
Position Responsibilities:
- Ensure clinical trial activities are compliant with ICH and applicable country regulations and guidelines and industry standards
- Align organization to ICH in implementing a quality culture from the outset of clinical trials to promote patient safety and data integrity
- Apply a risk-based approach by working collaboratively cross-functionally to ensure compliance
- Attend routine internal, external study team and ad hoc calls in support of ongoing quality oversight
- Engage partnership with external vendors via adherence to Quality Agreements and routine meetings
- Coordinate reviews, management documentation, track and/or follow-up on internal Quality Event investigations, deviations, Observations/Findings, CAPAs, etc. to ensure closure
- Support the use of an eQMS via data entry/document upload of quality activities (audits, observations, inspections, CAPAs, SOP Deviations, QEs/Investigations) and SOP updates
- Contribute to the annual audit plan
- Assure through Qualification audits and oversight activities that clinical trial vendors are operating in compliance with all applicable procedures, study documents, regulations/guidelines
- May review vendor MSA or contract/Work Orders
- Conduct or manage internal/external audits (vendor, site, document, system or process) and prepare or review audit reports
- Coordinate and manage services provided by external QA vendors
- Review key documents, such as IB, Protocols/Amendments, Consents, TMF Plans
- Inform and escalate to management in real-time or during routine updates, as appropriate
- Participate in inspection readiness activities or provide support during global agency inspections
- Conduct other tasks in support of GCP Quality activities, (e.g., chase training assignments, request contracts)
- Stay abreast of applicable global regulations, guidances, and industry best practices
Qualifications and Skills:
- Overall qualification by experience to support the responsibilities not limited to those outlined above
- Demonstrated GCP knowledge, GLP/GVP knowledge a plus
- Solid understanding of the cross-functional drug development process including specific to clinical trial operations, data management, statistics, etc.
- Skilled in developing collaborative internal and external relationships
- Business and Operational acumen to include escalation to management
- Ability to interact with all levels within an organization
- Experience in inspection preparation or supporting regulatory agency inspections
- Experience in using eQMS systems, such as Veeva
- BS in a scientific or other relevant discipline with equivalent work experience
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.