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Senior Manager, Clinical Partner Outsourcing
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Senior Manager, Clinical Partner Outsourcing
role at
BioSpace . By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life‑changing therapies to patients worldwide.
Objective / Purpose The Senior Manager, Clinical Partner Outsourcing (CPO) ensures seamless execution of clinical studies by developing robust supplier contracts through commercial negotiations and resolving commercial and operational challenges. This role is responsible for ensuring a high level of fiscal discipline and enhancing cross‑functional collaboration, and ensuring studies start on time, aligned to business requirements and Takeda standards and with the right commercial structures in place.
Accountabilities
Responsible for the development and finalization of study‑level contracts and change orders in partnership with key functions and aligned with Master Service Agreements, to ensure predictable delivery, quality and alignment to Takeda’s requirements, values and policies.
Lead ball‑parking, contracting and commercial management of complex clinical studies, understanding study requirements and translating into robust supplier contracts across a broad category of suppliers supporting R&D activities for assigned therapeutic areas and studies.
Apply appropriate commercial constructs, aligned to business requirements, to enable study start, even with evolving assumptions.
Utilize cost models and workbooks to validate contract pricing and budget assumptions for complex agreements and develop enhancements to improve validation capabilities.
Drive negotiations with CROs and suppliers to secure optimal terms for Takeda.
Manage contract amendments throughout the study lifecycle.
Support study teams in completing final reconciliation at study closeout.
Develop close collaborative working relationships with clinical operations and other key stakeholders to improve understanding and engagement.
Generate preliminary cost estimates to support Study Execution Teams (SET) in budget planning.
Collaborate with study teams to address commercial/contractual challenges, proactively identify potential issues, develop contingency plans and elevate to Clinical Partner Outsourcing/SPO leadership as necessary.
Escalate issues through the appropriate channels when local resolution is not achievable.
Drive operational support & issue resolution by supporting teams in addressing operational and performance‑related supplier issues.
Ensure consistency between contractual agreement and operational implementation.
Serve as an SME and lead continuous improvement initiatives to enhance performance and efficiency, identifying best practices through industry benchmarking.
As a member of the CPO team, anticipate and identify external industry trends impacting Takeda’s operating/cost model.
Ensure compliance with all applicable internal policies and procedures, regulations, support inspection readiness of all regulated activities.
Lead or participate in special projects and initiatives to support the business.
Education & Competencies (Technical And Behavioral)
Bachelor’s degree required; advanced technical degree (e.g., MBA) or certifications (e.g., PMP, CPA) preferred.
7+ years of experience in the pharmaceutical industry or clinical research environment.
Experience supporting a complex organization and demonstrated ability to work across functions and regions.
Proven experience in clinical procurement, contract management, or supplier relationship management.
Strong knowledge of clinical trial processes and regulatory requirements.
Experience in contract negotiations, financial analysis and budget management.
Familiarity with CRO and clinical outsourcing models, including financial and commercial constructs.
Sound understanding of GCP, ICH guidelines, and clinical trial regulations.
Strong strategic thinking and project management skills.
Excellent communicator with strong written and verbal presentation skills.
Additional Information
The position will be based in Cambridge, MA. This position is currently classified as “remote” by Takeda’s Hybrid and Remote Work policy.
Takeda Compensation And Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees and strive to be more transparent with our pay practices.
Location:
Boston, MA
U.S. Base Salary Range:
$137,000.00 - $215,270.00
U.S. based employees may be eligible for short‑term and/or long‑term incentives. They may also participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement Takeda is proud of its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations Boston, MA
Worker Type Employee
Worker Sub‑Type Regular
Time Type Full time
Job Exempt Yes
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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Senior Manager, Clinical Partner Outsourcing
role at
BioSpace . By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life‑changing therapies to patients worldwide.
Objective / Purpose The Senior Manager, Clinical Partner Outsourcing (CPO) ensures seamless execution of clinical studies by developing robust supplier contracts through commercial negotiations and resolving commercial and operational challenges. This role is responsible for ensuring a high level of fiscal discipline and enhancing cross‑functional collaboration, and ensuring studies start on time, aligned to business requirements and Takeda standards and with the right commercial structures in place.
Accountabilities
Responsible for the development and finalization of study‑level contracts and change orders in partnership with key functions and aligned with Master Service Agreements, to ensure predictable delivery, quality and alignment to Takeda’s requirements, values and policies.
Lead ball‑parking, contracting and commercial management of complex clinical studies, understanding study requirements and translating into robust supplier contracts across a broad category of suppliers supporting R&D activities for assigned therapeutic areas and studies.
Apply appropriate commercial constructs, aligned to business requirements, to enable study start, even with evolving assumptions.
Utilize cost models and workbooks to validate contract pricing and budget assumptions for complex agreements and develop enhancements to improve validation capabilities.
Drive negotiations with CROs and suppliers to secure optimal terms for Takeda.
Manage contract amendments throughout the study lifecycle.
Support study teams in completing final reconciliation at study closeout.
Develop close collaborative working relationships with clinical operations and other key stakeholders to improve understanding and engagement.
Generate preliminary cost estimates to support Study Execution Teams (SET) in budget planning.
Collaborate with study teams to address commercial/contractual challenges, proactively identify potential issues, develop contingency plans and elevate to Clinical Partner Outsourcing/SPO leadership as necessary.
Escalate issues through the appropriate channels when local resolution is not achievable.
Drive operational support & issue resolution by supporting teams in addressing operational and performance‑related supplier issues.
Ensure consistency between contractual agreement and operational implementation.
Serve as an SME and lead continuous improvement initiatives to enhance performance and efficiency, identifying best practices through industry benchmarking.
As a member of the CPO team, anticipate and identify external industry trends impacting Takeda’s operating/cost model.
Ensure compliance with all applicable internal policies and procedures, regulations, support inspection readiness of all regulated activities.
Lead or participate in special projects and initiatives to support the business.
Education & Competencies (Technical And Behavioral)
Bachelor’s degree required; advanced technical degree (e.g., MBA) or certifications (e.g., PMP, CPA) preferred.
7+ years of experience in the pharmaceutical industry or clinical research environment.
Experience supporting a complex organization and demonstrated ability to work across functions and regions.
Proven experience in clinical procurement, contract management, or supplier relationship management.
Strong knowledge of clinical trial processes and regulatory requirements.
Experience in contract negotiations, financial analysis and budget management.
Familiarity with CRO and clinical outsourcing models, including financial and commercial constructs.
Sound understanding of GCP, ICH guidelines, and clinical trial regulations.
Strong strategic thinking and project management skills.
Excellent communicator with strong written and verbal presentation skills.
Additional Information
The position will be based in Cambridge, MA. This position is currently classified as “remote” by Takeda’s Hybrid and Remote Work policy.
Takeda Compensation And Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees and strive to be more transparent with our pay practices.
Location:
Boston, MA
U.S. Base Salary Range:
$137,000.00 - $215,270.00
U.S. based employees may be eligible for short‑term and/or long‑term incentives. They may also participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement Takeda is proud of its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations Boston, MA
Worker Type Employee
Worker Sub‑Type Regular
Time Type Full time
Job Exempt Yes
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
#J-18808-Ljbffr