Regional Head of Clinical Operations, Southern and Central Eastern Europe

vor 1 Woche

Boudry, Schweiz Bristol-Myers Squibb Vollzeit
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Position Summary

The Regional Head of Clinical Operations, Southern and Central Eastern Europe provides site management and monitoring support within the Southern and Central Eastern European region and across the BMS R&D portfolio. This role reports to the Senior Vice President and is a key member of the RCO Leadership Team.

Key Responsibilities
  1. Provides strategic and operational leadership for site management and monitoring conducted within the region across the BMS R&D portfolio.
  2. Accountable to provide significant input, guidance, and direction to global initiatives to ensure that regional perspective and operational implications of proposed changes are considered and managed.
  3. Identifies needs, directing development and continuous improvement of processes, systems and strategies to support evolution of GDO business operating model with a particular focus on regional operational aspects.
  4. Leads a multi-national team of clinical operations professionals that contribute significantly to BMS portfolio of clinical trials.
  5. Provides ongoing feedback, coaching, and career development, including engagement and retention support to staff to maximize their potential.
  6. Empowers and holds country level clinical trial management to high quality performance and delivery of the business.
  7. Provides overall leadership and guidance across the portfolio that shapes the direction of RCO strategy to assure optimized geographic allocation of resources supported through internal resources & external partnerships.
  8. Ensures adaptive management of site monitoring and site management through the effective deployment of resources and streamlined processes, ensuring productivity targets, validity and quality of the data gathered in support of the evolving portfolio of BMS products.
  9. Understands the regulatory environment within the region, providing direction, guidance and support during inspection preparation, sponsor, and site activities.
  10. Represents the Company in key interactions with key external partners.
  11. Serves as a leader across R&D and develops strong and productive working relationships with key stakeholders throughout BMS.
  12. Ensures RCO representation as needed in governance or strategic teams or committees.
  13. Engages and energizes employees through communication of goals, priorities and other business critical information.
  14. Develops and promotes a workplace culture that values diversity of thought, promotes integrity and creates an atmosphere that supports coaching and fosters accountability.
Qualifications & Experience
Degree Requirements
  1. Bachelor's degree required with an advanced degree preferred.
Experience Requirements
  1. At least 10 to 15 years of relevant industry experience, with substantial experience of managing staff in a global setting.
  2. Significant global clinical trial expertise and a successful track record of leading through influence.
  3. A strong understanding of the drug development process with proven expertise in clinical trial execution and management in a global arena.
  4. Expert in ICH/GCP principles as it relates to clinical trial execution.
Key Competency Requirements
  1. Demonstrated partnership across various collaborative forums, CROs, SMOs and/or local site networks.
  2. Diverse and sufficient technical expertise to be a credible interface to all global development and business partners.
  3. Broad intelligence of the clinical trial environment across key regions.
  4. Strong influential leadership and communication capabilities.
  5. Knowledge, experience and successful interaction with important International Health Authorities.
Travel Requirements
  1. Up to 30% to 40% of travel required.
Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to gender identity, race, color, religion, sexual orientation, national origin or disability.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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