



Job Information
Takeda Pharmaceuticals Patient Recruitment and Retention Lead in Topeka, Kansas
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
Patient Recruitment and Retention Lead
Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Patient Recruitment and Retention Lead based remotely reporting to the Director, Patient Recruitment and Retention.
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 accomplish their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, 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 an important contributor to our inspiring, bold mission.
GOALS:
Oversee and provide quality patient engagement and recruitment services that allow study teams to meet patient enrollment goals.
Work to deploy new processes, methodologies, data and technologies for future implementation.
ACCOUNTABILITIES:
Oversee execution of patient recruitment deliverables by Specialist and other team members regarding operational planning activities supporting clinical project teams building phase 2 through phase 4 clinical research studies including:
Early operational planning
Protocol synopsis feasibility assessments
Site identification
Enrollment forecasting and modeling
Recruitment support strategies (e.g. central recruitment)
Recruitment and retention plans
Ensure delivery of high-quality and finalize subject recruitment and retention plans in collaboration with the Takeda clinical project teams/study team and contracted supplier(s) before First Patient First Visit.
Report on and apply best-practice examples and lessons learned regarding recruitment and retention practices.
With Team Lead, performs co-management of Recruitment Vendor Management Strategy (RVMS) to:
Manage quantitative decision support framework for strategy development, vendor selection, and objective setting.
Manage contract and vendor relationship framework to align with adherence to RVRM and quantitative decision support framework.
Attend Relationship Management Committees with recruitment vendors to assess and communicate the effectiveness of these relationships to applicable recruitment strategies.
Systematically evaluate and communicate financial impact of specialist vendor (recruitment and retention) and recruitment strategies to important partners.
Build daily delivery of activities as described above supporting clinical programs ( e.g. including delivery of decision support data and methodologies for protocol development, site selection and management of recruitment support vendors.
Support Director with activities related to:
Process improvement and mapping
Training
Inter-departmental collaboration (e.g. Compliance, DSI technologies)
Vet new 3rd party providers or patient engagement models
Internal performance metrics
EDUCATION AND SKILLS:
Bachelor's Degree.
5 or more years of experience in patient recruitment with evidence of increasing responsibility within a pharmaceutical company, CRO or similar organization.
Expertise in developing recruitment and retention strategies, country/site identification, and generation of material and trial metrics.
Successful leadership, and development of large, diverse globally dispersed teams experience.
Knowledge of leading edge trial optimization vendors, tools, and methods.
Knowledge of current regulatory requirements and guidelines governing clinical research.
Experience in process design and improvement .
Understanding of clinical trials, relevant knowledge of GCP/ICH and applicable global regulations with regard to trial optimization strategies.
WHAT TAKEDA CAN OFFER YOU:
Base Salary Range: $160,000 to $180,000. Employees may also be eligible for Short Term and Long-Term Incentive benefits. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off.
The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience.
This posting is made in compliance with Colorado's Equal Pay for Equal Work Act, C.R.S. § 8-5-101 et seq.
Empowering Our People to Shine
Discover more at takedajobs.com
No Phone Calls or Recruiters Please.
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 - Virtual
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
#LI-Remote