Job Description:
This role is a hybrid position which requires a minimum of 3 days on-site in one of two possible locations: Basking Ridge, NJ or Armonk, NY.
Remote work is not an option for this role.
Responsibilities:
* Lead and implement the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM).
* Responsible for clinical operations activities and decisions including quality, timelines, and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations, and company Standard Operating Procedures (SOPs) within assigned program(s).
* Interact with senior level management, external vendors, collaboration partners, and clinical study personnel for clinical research project and department initiatives.
* Line management of clinical trial management staff, including recruitment, development, coaching, mentoring, and performance management.
* Drive the functional strategy of Clinical Trial Management in partnership with Functional leadership.
Key Skills and Qualifications:
* Advanced interpersonal and leadership skills.
* Ability to provide operational strategic direction and guidance for clinical programs.
* Applies sophisticated technical knowledge to solve highly complex issues.
* Understanding of relevant industry trends.
* Strong analytical skills with a data-driven approach to planning, executing, and problem-solving.
* Advanced interpersonal skills via verbal, written, and presentation abilities.
* Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization.
* Influence and negotiate across a wide range of senior partners.
* Budget management expertise and strong financial competence.
* Consistent track record of building, leading, and developing productive teams and collaborations.
* Expert project management skills, cross-functional engagement, and organizational skills.
To be considered, you must have a Bachelor's degree and a minimum of 12 years of relevant pharmaceutical industry experience, 8 years within Clinical Trial Management. Experience with early phase clinical trials is highly preferred.