Dir, Epidemiology Pipeline (TA-Oncology)

Job Responsibilities

Serves as a 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 oversight of selected projects, responsible for meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction.

Covers the scientific aspects of study start-up and ongoing study management. Leads the development of and/or peer-review 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 reports/manuscripts/abstracts/presentations.

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 develops trainings for RWLP/Company organization to enhance their familiarization of epidemiologic study designs and applicable guidelines.

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.

Works to develop collegial relationships with sponsors, thought-leaders and clinical investigators.

Develops abstracts, provides podium presentations, and leads authorship of articles, manuscripts, etc. in industry and peer-reviewed journals to promote Company services.

Requirements

• SME in Oncology Clinical Trials
• Requires graduate degree in Epidemiology, Statistics, or Public Health; (Masters; Preferred Doctorate)
• Requires in-depth knowledge of and experience with a variety of study designs; familiarity with post-marketing and late phase study designs as well as relevant guidelines preferred
• Requires basic knowledge of statistical programming language(s) (e.g., SAS, R, Python)
• Excellent communication, presentation, both written and spoken
• Strong personal communication and team-oriented skills
• Demonstrated leadership and technical skills

Qualifications

• Graduate degree in Epidemiology, Statistics, or Public Health; (Masters; Preferred Doctorate)
• In-depth knowledge of and experience with a variety of study designs; familiarity with post-marketing and late phase study designs as well as relevant guidelines preferred
• Basic knowledge of statistical programming language(s) (e.g., SAS, R, Python)
• Excellent communication, presentation, both written and spoken
• Strong personal communication and team-oriented skills
• Demonstrated leadership and technical skills

Benefits

• Health benefits to include Medical, Dental and Vision
• Company match 401k
• Eligibility to participate in Employee Stock Purchase Plan
• Eligibility to earn commissions/bonus based on company and individual performance
• Flexible paid time off (PTO) and sick time

Pay

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Schedule

N/A