Associate Director - Feasibility

March 1

🍂 Massachusetts – Remote

Although this job is listed in Massachusetts, this company may be open to hiring remote in other states.

💵 $149.1k - $234.3k / year

⏰ Full Time

🟠 Senior

👔 Director

🦅 H1B Visa Sponsor

Apply Now

Receive Emails with Similar Jobs

Takeda

WebsiteLinkedInAll Job Openings

Takeda is a global biopharmaceutical company dedicated to bringing better health and a brighter future to patients worldwide. With a strong focus on research and development, manufacturing, and quality, Takeda operates with a commitment to ethics and a diverse workforce that spans over 80 countries. The company leverages innovative science and partnerships to create impactful medicines, including therapies in oncology and vaccines, ensuring that they effectively meet the needs of the patients they serve.

Pharmaceuticals • Therapeutics • Oncology • Gastroenterology • Vaccines

10,000+ employees

Founded 1781

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

💰 Grant on 2016-08

📋 Description

• Manage feasibility activities at a program and/or asset level with minimal oversight. • Conduct data-driven feasibility assessments for Phase I – IV clinical studies. • Utilize internal and external competitive intelligence to develop benchmark assumptions. • Collaborate with operational leads to increase understanding of metrics and forecasts. • Contribute in efforts to implement innovative processes and technologies. • Participate in or lead global initiatives supporting Takeda R&D objectives. • Ensure consistent standards are applied to the feasibility process across the portfolio. • Develop TA/Indication expertise and act as feasibility subject matter expert. • Lead country and site selection process to ensure data-driven decisions. • Regularly review ongoing study performance in relation to projected study timelines.

🎯 Requirements

• BS degree or international equivalent in a life science required, advanced degree preferred. • 8 or more years of experience in Clinical Operations, Data Analytics, global feasibility, and trial optimization required. • 7 or more years of direct responsibility in leading strategic feasibility assessments of global clinical research studies. • Experience with leading edge trial optimization vendors, tools, and methods. • Proficiency with software models and database structures. • Expertise in principles of data-driven country/site identification and selection. • Ability to manage and collaborate in a matrix work environment. • Extremely proficient with MS Office applications.

🏖️ Benefits

• Eligible for short-term and/or long-term incentives. • Eligible for medical, dental, vision insurance, and 401(k) plan. • Eligible for basic life insurance and tuition reimbursement program. • Paid volunteer time off and company holidays. • Up to 80 hours of sick time per calendar year. • Accrue up to 120 hours of paid vacation.