Director, Clinical Operations

Deciphera Pharmaceuticals; Waltham (MA); On-site; USD 186,000 - 255,000; Full time

Job summary

Deciphera Pharmaceuticals seeks a Director of Clinical Operations to lead and manage clinical stage programs. This role involves strategic leadership, ensuring quality standards, and overseeing the execution of clinical trials. The ideal candidate will have extensive experience in clinical trial management and be capable of fostering a collaborative team culture.

Benefits

Competitive salary and annual bonus.

Comprehensive benefits package including medical, dental, and vision insurance.

Generous parental leave and family planning benefits.

Qualifications

• 12+ years of experience, with a minimum of 10 years in clinical trial management.
• Expertise in clinical development process and global regulatory requirements.

Responsibilities

• Develop and execute clinical program strategy.
• Lead and manage the clinical operations team for assigned program(s).
• Ensure clinical trials are properly defined, planned, and executed.

Skills

Leadership

Communication

Organizational skills

Education

Bachelor's or Master's degree in health science or related field

Job description

1 week ago Be among the first 25 applicants

Job Description

The Director, Clinical Operations will ensure that clinical stage programs achieve program objectives within established timelines, budget, and quality standards. This role involves contributing to the development of clinical program strategy, providing leadership to the clinical operations team, and ensuring superior execution and transparency within the department.

Job Description

The Director, Clinical Operations will ensure that clinical stage programs achieve program objectives within established timelines, budget, and quality standards. This role involves contributing to the development of clinical program strategy, providing leadership to the clinical operations team, and ensuring superior execution and transparency within the department.

Key Responsibilities

• Develop and execute clinical program strategy
• Lead and manage the clinical operations team for assigned program(s)
• Ensure clinical trials are properly defined, planned, and executed
• Assist in authoring key regulatory documents
• Ensure study objectives align with clinical development strategy and corporate goals
• Manage external vendors to deliver within timelines and budget
• Foster a collaborative culture and serve as a leadership role model
  
  

Qualifications

• Bachelor's or Master's degree in health science or related field
• 12+ years of experience, with a minimum of 10 years in clinical trial management
• Expertise in clinical development process, global regulatory requirements, and CRO/vendor management
• Excellent leadership, communication, and organizational skills
  
  

Additional Information

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $186,000.00 - $255,000.00. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.

Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable).

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
• Generous parental leave and family planning benefits.
• Outstanding culture and opportunities for personal and professional growth.
  
  

Apply Now: Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!

EQUAL EMPLOYMENT OPPORTUNITY INFORMATION

Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Pharmaceutical Manufacturing

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