Bristol Myers Squibb Associate Director - Global Quality Clinical Trials and Safety in Princeton, New Jersey
Purpose/Objective of the job
· Conduct Good Clinical Practice (GCP) and pharmacovigilance (PV) audits as above described.
· Act as project-specific liaison between R&D Quality - CT&S and key stakeholders, including Global Clinical Operations and Global Regulatory, Safety & Biometrics (GRSB) personnel, monitoring the status of the project(s) to plan audits and assuring GQ - CT&S leadership as informed.
· Represent GQ-CT&S as an expert in specific GCP/PV related areas
Key Responsibilities and Major Duties
· Within multiple areas of GCP/PV expertise, act as an expert resource;trainer for GQ-CT&S and as liaison with key stakeholders to provide input into related audit strategy and plans
· Within areas of expertise, maintain awareness of trends and new developments internally and externally
· Perform GCP and PV audits, including audits of clinical investigator sites, vendors, internal systems and clinical study reports to assess regulatory compliance;
· Apply audit principles, procedures, and methods; Collect information through effective interviewing, listening, observing and reviewing documents, records and data;
· Prioritize and focus on matters of significance;
· Confirm the sufficiency and appropriateness of audit evidence to support audit findings and conclusions;
· Assess those factors that may affect the reliability of the audit findings and conclusions;
· Prepare clearly-written, concise, accurate and evidence-based audit report;
· Maintain audit database
· Review and assess (or support the review) received corrective and preventive action plans according to specified timelines to ensure resolution of audit findings and prevent recurrence.
· Maintain an in-depth knowledge of governmental regulations impacting clinical research and PV and development of medicines.
· Provide advice and counsel concerning GCP regulatory requirements.
· Act as project-specific liaison (Project Coordinator) and provide input into audit plans and strategy.
· Regularly evaluate key PV and clinical research processes to determine compliance with regulatory requirements and established standard operating procedures.
· May provide mentoring for new GQ-CT&S staff, as needed.
· Support upper management on the on-boarding of new hires
· Represent GQ-CT&S position during internal and external meetings
· Lead project related teams or workstreams as assigned
· Act as an advisor and back up to the Director
· Coordinate health authority inspections as assigned and maintain inspection tools repository
Key Stakeholders/Contacts -
· Regular contact and collaboration with Global Quality CT&S strategy roles, GQ and Clinical Quality governance (risk management and CAPA), colleagues/co-auditors located globally;
· Contact with appropriate technical, supervisory and management personnel internally and externally (investigator sites, vendors, etc.) in the conduct and reporting of audits.
· Regular collaboration with GQ-CT&S colleagues and with GCO and GRSB personnel
· Possible interactions with external auditors and Regulatory Agency inspectors during the conduct of health authority inspections either at clinical sites or at BMS facilities.
· Miscellaneous contacts as assigned by GQ-CT&S management
List of minimum requirements
o Bachelor´s degree required - Life Sciences degree preferred
o Experience/Responsibility and minimum # of years:
o Demonstrated expertise and specific technical knowledge of the GCP and PV areas subject to audit, as evidenced by at Ieast 8 years in the pharmaceutical industry
o Minimum 5 years technical auditing and/or related experience; PV and GCP auditing preferred
o Strong skill in risk based prioritization
o Strong critical thinking to analyze complex situations and discern critical issues and non-compliant situations and to recommend appropriate corrective and preventive actions;
o Excellent understanding of the drug development process and end to end quality process
o Support GQ-CT&S management on identification of areas to increase department efficiency
o Demonstrates computer literacy and is able to function independently within an environment that relied heavily on technology for information and communication
o Excellent oral and written communication;
o Fluent in English (and other languages, as applicable to assigned audit region);
o Sense of diplomacy and discretion;
o Maintains the confidentiality and security of information, data and records;
o Demonstrates commitment to delivering high-quality work product;
o Knowledge of governmental regulations impacting clinical research and drug development
o Understand the appropriateness and consequences of using sampling techniques for auditing;
o Ability to make ethical, scientifically sound recommendations, consistent with company policy/strategy and cost effective;
o Demonstrates flexibility, open-mindedness and adaptability to a rapidly changing environment;
o Develops strong working relationships with key stakeholders;
o Ability to manage competing priorities.
o Ability to lead change process within functional group
o Possesses detailed knowledge of areas of expertise and could teach or mentor others
o Develops and applies new methods and ideas to enhance performance
BMS Behaviors and Working conditions :
o BMS Biopharma Behaviors required: Passion, Accountability, Innovation, Speed
o Travel Required (nature and frequency) approximately 25% travel to perform audits and attend professional meetings and seminars.
o Overnight Absences Required (per typical month): Approximately 5 days per month
Software that must be used independently and without assistance (e.g., Microsoft Suite, Electronic Trial Master File, Oracle clinical database, RAVE, Trackwise, Sharepoint, etc
Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.