Sr Director, Epidemiology RWE

Syneos Health Careers$160K — $200K *
US-AnywhereRemote in Ontario, CA
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. or equivalent in epidemiology or related scientific discipline
  • 5+ years of experience in real-world evidence (RWE) research
  • Expertise in clinical and epidemiological practice guidelines
  • Strong background in clinical research models and protocol design
  • Excellent communication and presentation skills for diverse audiences
  • Proven leadership in managing complex scientific projects
  • Experience in developing proposal strategies and client relationships

Responsibilities

  • Lead scientific consulting for RWLP management and senior executives
  • Develop and secure global business opportunities through collaboration
  • Ensure scientific oversight and exceed client expectations for project deliverables
  • Guide the creation of scientific publications and presentations
  • Improve organizational capacity and operational methodologies
  • Facilitate scientific advisory boards and produce relevant documents
  • Consult on clinical programs and regulatory issues with stakeholders

Benefits

  • Flexible work environment
  • Opportunities for professional growth and training
  • Collaboration with leading experts in the field
  • Exposure to a wide range of therapeutic areas and drug development processes
Full Job Description
Description
Sr Director, Epidemiology RWE

Job Responsibilities

  • Serves as the lead scientific resource for RWLP management, Company senior management, and other Functions within Company providing expertise in multiple scientific areas.
  • Works hand-in-hand with RWLP management, business development, and operations personnel to develop and win global business opportunities; helps to lead the development and delivery of project proposals, bid defenses, and represents capabilities presentations.
  • Provides overall scientific executive oversight of selected projects, responsible for meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction.
  • Guides the development of abstracts, podium presentations, and authorship of articles, manuscripts, etc. in industry and peer-reviewed journals to promote Company services in alignment with sales and marketing strategy.
  • Responsible for the continued building of organizational capacity, improvement of scientific and operational processes and methodologies for non-traditional site management tasks (i.e., remote or central monitoring approaches, minimized regulatory document collection, etc.), integrated RWLP technology solutions including secondary database resources, and RWLP Standard Operating Procedures (SOP) development and maintenance.
  • Works collaboratively across the organization to help develop business opportunities in the area of post marketing safety commitments and/or risk management; develops and recommends techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
  • Provides executive oversight of the scientific aspects of study start-up and ongoing study management including review/design/consultation of essential study documents including the protocol, case report forms, statistical analysis plan, study management plans, and interim/final study reports. Facilitates scientific advisory boards for safety studies and produces scientific documents.
  • Maintains a strong working understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real-world research development trends, and regulatory expectations and guides the development of trainings for RWLP/Company organization to enhance their familiarization of epidemiologic study designs and applicable guidelines.
  • Works to develop collegial relationships with sponsors, thought-leaders and clinical investigators.
  • Provides consulting, as appropriate to sponsors and regulatory authorities on a variety of topics, including clinical program and protocol design, operational issues, scientific programs/publications, advisory boards, medical/safety/ethical issues, etc.


Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms.

Summary
Responsible for providing leadership and strategic direction from a scientific perspective as a member of the Real World and Late Phase (RWLP) management team. Serves as a scientific expert offering organizational infrastructure and business development support, and study design consultation while raising awareness of RWE across the enterprise.

About Syneos Health Careers

Syneos Health Careers

Joining Syneos Health presents an unparalleled opportunity to become part of a global team of professionals dedicated to biopharmaceutical solutions. At Syneos Health, job opportunities abound, offering a gateway to enhancing career paths in a company celebrated for its commitment to therapeutic and operational excellence.

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