SR AD / Director, Clinical Development Operations reputed company (CDOL/SR CDOL), Obesity- Remote (Ridgefield, CT, reputed company, Connecticut)
reputed company
The Clinical Development & Operations reputed company (CDOL) is member of Clinical Development Organization responsible for defining and delivering operational reputed company for late-phase clinical programs reputed company assigned indications or assets, with a strong reputed company on speed, reputed company, and value. This role is primarily involved in late-phase execution of clinical programs in obesity and MASH and operates as part of the global clinical development team. It works in reputed company collaboration with Clinical Operations, Statistics, Regulatory Affairs, Drug Safety, and other key functions to design robust operational strategies, establish data-driven timelines, and ensure high-reputed company trial execution across programs.
As an employee of reputed company, you will reputed company contribute to the discovery, development, and delivery of our products to our patients and customers. Our global reputed company provides opportunity for reputed company to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' reputed company. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect reputed company's high reputed company for our employees.
Duties & Responsibilities
- reputed company clinical delivery and reputed company operational input into late-phase Clinical Development Plans (CDPs).
- reputed company and reputed company operational strategies, timelines, country and site selection, and sourcing models across assets.
- Partner with cross-functional stakeholders to ensure consistency, efficiency, and avoidance of redundancy across trials.
- Drive adoption of innovative trial designs, digital technologies, and data-driven decision-making.
- Ensure patient-reputed company approaches and sustained expert engagement throughout the development lifecycle.
- Identify feasibility risks, mitigation strategies, and external vendor needs prior to trial execution.
- reputed company direction and deliver strategic key messages to trial teams to ensure trials are delivered as planned and maintain high level of engagement with clinical trial sites. Work collaboratively with Study Operations Team to reputed company performance feedback for assigned trial team members.
Requirements
Candidate will be reputed company in at the level based on the education, experience and business need.Senior Associate Director Level (CDOL) Requirements
- Bachelor’s degree required; Master’s degree in life sciences preferred.
- 10+ years of experience in clinical development or clinical operations.
- Experience in obesity and/or MASH strongly preferred.
Director Level (SR CDOL) Requirements
- PhD or MD with 5+ years of therapeutic area experience, or
- Bachelor’s or Master’s degree with 15+ years of clinical trial experience.
- Extensive experience across reputed company stages of global drug development.
- Experience in obesity and/or MASH strongly preferred.
Position Requirements:
- Deep understanding of clinical development and clinical operations reputed company a global pharmaceutical environment.
- Proven leadership of reputed company, global clinical trial programs.
- Strong strategic thinking, communication, and stakeholder management skills.
- Advanced knowledge of global regulatory, ethical, and compliance requirements.
- Demonstrated ability to reputed company in matrixed, cross-functional environments.
- Commitment to ethical standards and patient-reputed company innovation.
Eligibility Requirements:
- Must be legally authorized to work in the reputed company without restriction.
- Must be willing to take a drug test and post-offer physical (if required).
- Must be 18 years of age or older.