Clinical Project Management Director - CNS

仕事内容

IQVIAs Central Nervous System Unit is a global team of professionals dedicated to assisting our clients in driving healthcare forward and enabling medical breakthroughs that advance healthcare and patient treatment options around the world, We are looking for an Clinical Project Management Director with experience in Neurology, Neuro-Degenerative Diseases, Psychiatry, Pain or Rare CNS-Related Diseases experience to join our innovative and dynamic group.

This is an important and high-profile role within IQVIA. Clinical Project Management Directors direct and manage the team responsible for clinical delivery of complex; global full service, multi-regional studies and/or programs. They have strategic decision-making responsibility for the project/program.

As a Clinical Project Management Director, you’ll be responsible for the direction and management of portfolios and/or accounts from an operational perspective, ensuring that studies and/or programs are delivered on time and quality resulting in strong financial performance and customer satisfaction in accordance with SOPs; policies and practices from pre-award to close-out. You’ll leverage your therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.

The dedicated CNS unit sits within IQVIA’s global Project Leadership organization; as a member of this group, you will be responsible for delivery of global and/or regional studies and / or critical process and vendor management in a variety of indications. Our CNS team is growing quickly, and candidates with experience in the following experience can expect to have a strong impact:

• Neurology,
• Neuro-Degenerative Diseases,
• Psychiatry,
• Pain or Rare CNS-Related Diseases
  

You will need to be comfortable collaborating and communicating with a variety of colleagues and clients and demonstrate flexible and creative leadership. Global experience and a biopharmaceutical, CRO or related vendor (IP supply, clinical laboratory, etc.) is ideal.

While project assignments vary, your typical responsibilities might include:

• Contribute to the development of the project delivery strategy for Request for Proposals (RFPs). Participate in bid defense preparations. Lead bid defense presentations in partnership with business development for large, complex, multi-service, multi-region studies or programs. Understand project strategy and operationalize the agreed upon approach.
• Direct the execution of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Recognize systemic issues at program or portfolio level and identify solutions with the project teams, recommend actions to improve efficiencies and oversee the implementation of best practices, address escalation items with the customer.
• Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Responsible for the management and delivery of large and/or complex studies or programs of studies.
• May be responsible for portfolio management with one customer or therapeutic area.
• Serve as primary project/program/portfolio contact with customer and own relationship with key customer contact(s), communicate/collaborate with IQVIA business development as necessary.
• Forecast and identify opportunities to accelerate activities to bring revenue forward and identify new business opportunities.
  

Minimum Required Education And Experience

• Bachelor’s degree in life sciences or related field and 12 years’ clinical research experience including 6 years’ project management experience and experience in clinical operations; or equivalent combination of education, training and experience.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements, i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired. Knowledge of clinical trials - Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.
• Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently. Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Excellent customer management skills and demonstrated ability to understand customer needs Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. Good understanding of other IQVIA functions and their inter-relationship with Project Leadership.
• Finances - Good understanding of project financials including experience managing, contractual obligations and implications.
  

Physical Requirements

• Extensive use of keyboard requiring repetitive motion of fingers.
• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
• Regular sitting for extended periods of time.
• May require occasional travel.
  

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

https://jobs.iqvia.com