Clinical Project Manager – Oncology Trials – Takeda Pharmaceuticals (Cambridge, MA)
130000.00 $
Published date: 2025/04/26
- Location: Cambridge, Massachusetts, United States
Takeda Pharmaceutical jobs Cambridge MA
Location: Cambridge, Massachusetts
Company: Takeda Pharmaceuticals
Salary: $110,000 – $130,000/year + performance bonus
Job Type: Full-Time, Hybrid (2–3 days on-site)
Schedule: Monday to Friday
Job Description:
Takeda Pharmaceuticals is hiring a Clinical Project Manager to oversee oncology clinical trials within its global development programs. This role ensures clinical studies are conducted on time, within budget, and in compliance with regulatory requirements.
Key Responsibilities:
– Lead cross-functional study teams and manage vendor relationships
– Develop and manage study budgets, timelines, and risk assessments
– Support regulatory submissions and protocol development
– Ensure compliance with ICH GCP and Takeda SOPs
Requirements:
– Bachelor’s degree in Life Sciences or a related field (Master’s preferred)
– 4+ years of clinical trial management experience (oncology experience preferred)
– Knowledge of FDA, EMA, and ICH guidelines
– Strong project management, communication, and leadership skills
Benefits:
– Health, dental, vision, and life insurance
– Paid parental leave and wellness programs
– Tuition reimbursement and internal leadership development
– Hybrid work model and global career mobility opportunities
Location: Cambridge, Massachusetts
Company: Takeda Pharmaceuticals
Salary: $110,000 – $130,000/year + performance bonus
Job Type: Full-Time, Hybrid (2–3 days on-site)
Schedule: Monday to Friday
Job Description:
Takeda Pharmaceuticals is hiring a Clinical Project Manager to oversee oncology clinical trials within its global development programs. This role ensures clinical studies are conducted on time, within budget, and in compliance with regulatory requirements.
Key Responsibilities:
– Lead cross-functional study teams and manage vendor relationships
– Develop and manage study budgets, timelines, and risk assessments
– Support regulatory submissions and protocol development
– Ensure compliance with ICH GCP and Takeda SOPs
Requirements:
– Bachelor’s degree in Life Sciences or a related field (Master’s preferred)
– 4+ years of clinical trial management experience (oncology experience preferred)
– Knowledge of FDA, EMA, and ICH guidelines
– Strong project management, communication, and leadership skills
Benefits:
– Health, dental, vision, and life insurance
– Paid parental leave and wellness programs
– Tuition reimbursement and internal leadership development
– Hybrid work model and global career mobility opportunities
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