
Senior Manager, Study Management
Remote- Job Level: Senior
- Travel: Minimal (if any)
Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.
In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.
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Job Description
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world.
Here, you will be a necessary contributor to our inspiring, bold mission.
GOALS:
- Responsible for direct line management of assigned study management team members for a given therapeutic area(s).
- Ensuring appropriate training of study management team members in order to deliver operational consistency and high quality support across clinical trial programs.
- Provide guidance and mentorship to support the development of skills, knowledge, and expertise.
- Supporting the execution of studies in a matrix management structure to ensure compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs).
- Serves as subject matter expert to support complex activities such as process development, complex program support or department and/or business critical initiatives and deliverables.
ACCOUNTABILITIES:
- Provide direct supervision of study management team members within assigned TA, including hiring/staff selection and assignment of individual studies, resource allocation, onboarding, overall training, completion of goals, development plans, performance reviews, and Talent Management.
- Overseeing study management team members to ensure proper execution of assigned studies.
- Responsible for ensuring compliance of assigned team members to Takeda SOPs and training of systems and quality standards, including inspection readiness in execution of Takeda studies and trials.
- Responsible for training, coaching and mentoring study management team members and new hires in navigating career progression options within Takeda.
- Provides performance feedback on an ongoing basis to support continued development growth.
- Demonstrate leadership to direct reports, ensuring employees adhere to corporate policies and following up with management as appropriate.
- Ensure compliance with pre-defined roles and responsibilities within a matrix management structure.
- Contributes to resource evaluations for study to ensure adequate resources are available for the successful delivery of clinical programs.
- Maintain a positive, results-orientated work environment, building partnerships and modeling teamwork, communicating with the teams and stakeholders in an open, balanced, and objective manner.
- Support Global Clinical Development Operations (GCDO) initiatives (including lessons learned/best practices process) to develop innovative processes and technologies to advance operations, ensure compliance and quality delivery, and reduce operating costs; Support cross-functional strategic initiatives and processes.
- Foster knowledge sharing and the use of best practices across the study management team and act as team superuser or subject matter expert for the company systems and processes.
- May directly support Clinical Operations Program Leads in day-to-day activities for complex and/or business-critical clinical studies (including providing clinical study management expertise, study and CRO oversight, issue escalation, and resolution).
- Act as a role model for Takeda´s values.
EDUCATION AND EXPERIENCE:
- Bachelor’s Degree or international equivalent required, Life Sciences preferred. Advanced degree is highly desirable.
- 8 or more years experience in the pharmaceutical industry and/or clinical research organization.
- Prior experience in line management preferred and/or leadership experience as a mentor/supervisor or cross functional matrix leadership.
- Familiar with requirements for clinical trials (ICH/GCP) and regulatory submissions.
- Ability to manage a team to meet company objectives.
- Ability to work independently, take initiative, establish priorities, complete tasks to deadlines.
- Strong communication skills and customer focus with ability to interact in a global, cross-functional organization.
- Proven ability to communicate effectively and respond to inquiries and concerns, support issue escalation and proprose mitigation strategies where feasible.
- Must be able to work in a fast-paced environment with demonstrated ability to prioritize multiple competing tasks and demands.
- Demonstrated ability to be flexible and to adapt quickly to change.
- Excellent teamwork, organizational, interpersonal, and problem solving skills.
- Fluent business English (oral and written).
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 we strive to be more transparent with our pay practices.
For Location:
Massachusetts - VirtualU.S. Base Salary Range:
$137,000.00 - $215,270.00The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/or long-termincentives. U.S.based employees may be eligible to 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 in 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
Massachusetts - VirtualWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeJob Exempt
YesIt 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.#LI-Remote
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