At Intercept, we foster an environment that celebrates creativity, collaboration and mutual respect. We never hesitate to lean on our teammates and work together. Our relatively small size means you partner with accessible leaders who know you by name. This brings accountability and growth, which all add up to more opportunities to learn something new every day. A strong commitment to diversity, equity and inclusion is engrained in both our culture and our business. For self-motivated leaders who are ready to make a difference in the lives of patients, Intercept is a great place to be.
As Intercept continues to build its position as the leader in progressive non-viral liver disease, we are seeking an experienced Manager, Quality Assurance GCP. The position will be responsible to assess compliance with Intercept standard operating procedures, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with Clinical Development, Clinical Operations, CROs and Clinical Research Sites to provide quality oversight and collaboration on quality issues. This person is expected to play a major role in supporting the global inspection readiness strategy. Responsibilities include acting as an SME on the audit programs; internal systems, supplier, and of clinical trial sites. We are looking for a candidate with strong communication skills (written and verbal), with the ability to build internal and external relationships.
The successful candidate must be able to perform each of the following satisfactorily:
- Maintain GCP/ICH compliant systems and processes which control the quality of work and clinical trials conducted by Intercept in Europe.
- Lead GCP audits of Intercept research activities impacting clinical trials to assess compliance with study protocols, company procedural documents and relevant regulations and guidelines. Audits include investigator site audits, vendors and internal processes/systems.
- Quality collaboration on Intercept clinical SOPs and support continuous process improvements
- Support CRO quality agreements aimed at ensuring quality standards are established, effectively monitored and issues are resolved promptly and effectively.
- Report significant clinical quality deficiencies and/or risks to QA management.
- Represent the Quality function on the study teams and manage direct relationship with CROs and indirectly with all clinical sites.
- Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, and Medical Affairs.
- Support Internal Quality Audits against company Annual Audit Plan, CAPA Development, Effectiveness Checks and Oversight, Quality Management Reviews.
- Support efforts to prepare company and clinical sites for government regulatory agency visits to include local and potentially foreign government agencies; participate as Subject Matter Expert during regulatory GCP inspections
- Support training of Intercept staff on Intercept procedures, GCP regulations, and documentation systems to assure compliance with company policies and regulatory standards as it relates to Clinical Quality.
- Perform other related duties as assigned.
- Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
- Drive the spirit of "ONE Team" across all functions by supporting a team approach to focus on our patients and customers as our top priorities
- Make Intercept a truly desired place to work
Experience and Skills
- Bachelor's degree in science or equivalent.
- Minimum of 7 years of experience in a regulated environment related to pharmaceutical/biotech industry; experience in Clinical Quality Oversight required
- Minimum of 5 years of experience specific to Quality Assurance GCP
REQUIRED KNOWLEDGE AND ABILITIES:
- A strong understanding and knowledge of GCP/ICH regulations and an ability to apply them to clinical research and/or related processes is required.
- CAPA Development and Management experience.
- Inspection experience in supporting the facilitation of regulatory authority inspections.
- Excellent organization and multi-tasking skills.
- Exceptional interpersonal skills and problem-solving capabilities.
- Proven negotiation skills.
- Ability to work effectively across a matrix organization.
- Ability to work independently and prioritize with minimal daily instruction.
- Ability to think strategically in order to improve current processes.
- 20% travel is expected.
- Strong verbal and written communications skills
- Learning agility and ‘scalability’ to take on increasing responsibility as Intercept grows
- Consistent demonstration and embodiment of company core values: Collaboration, Excellence, Innovation, Integrity, Passion, Patient/Stakeholder Centricity
- Ability to have fun and thrive in a growing, diverse and inclusive work environment