Senior Manager, Study Site Engagement
Takeda · United States · 2 mo ago
RemoteRemoteBusiness DevelopmentFull-time
Objectives/Purpose
The Senior Manager, Study Site Engagement is the local face of Takeda by contributing to an effective partnership between Takeda study teams, study sites and the Clinical Research Organization (CRO) (i.e., the Clinical Research Associate (CRA)/Monitor).
This highly visible, field-facing role combines scientific understanding, operational expertise, and relationship-building to enhance site engagement across the full clinical trial lifecycle, from feasibility and site selection through study conduct and completion.
Accountabilities
Study Specific Engagement Activities:
Early engagement - Country and Site Feasibility
- Supports the Study Site Engagement Lead (SSEL)/ SSE Program Lead (SSE-PL)/SSE Study Lead (SSE-SL with the development of study site list for feasibility - site selection and aids in tracking feasibility progress and escalations for SSEL/LOC support.
Reports any discrepancy on feasibility progress to SSE-PL/SSE-SLL
- Liaises with SSE-PL/SSE-SL, MA, local Clinical Operations team (if available) and CRO staff for site identification and feasibility support in alignment with global study team.
Attends Pre-Study Visit (PSV) as requested or agreed upon with the SSE-SL.
- Helps to follow up with country MA, local Clinical Operations team and keep track country and site selection activities.
Study Startup Phase - Post Site Selection to Site Initiation
- Supports the SSE-PL/SSE-SL in tracking start-up hurdles escalated to the team and their resolution to ensure Site Initiation Visits (SIVs) and site activations are achieved as planned.
Attends and/or supports SIVs.
- Helps SSE-PL/SSE-SL in tracking resolution of any follow-up item needed post SIV until resolved by site and or CRO/Takeda study team.
As invited, attends Investigator Meetings (in the region) and liaises with sites / CRO.
- Regularly interacts with priority sites in assigned trials.
Enrollment and Study Conduct Phase
- Supports recruitment strategy and activities when targets are not met (e.g. utilization of Patient Recruitment & Retention materials, booster visits, phone contacts).
Interacts closely with local CRO team throughout the lifecycle of the study.
- Supports Takeda study teams as part of their day-to-day responsibilities and may act as an SSE-Study Lead (SSE-SL).
Training Applicable local regulations
- SOP trainings (Takeda and CRO, as applicable)
- TA/Study specific training
Non-Study Specific Engagement activities:
- Participation in following activities may vary depending on assignment by Line Manager:
- SSE Study Lead for assigned programs
- Helps to develop the global Site Engagement Strategy for the assigned trial, adapting it as necessary to meet specific requirements of each country.
- Attends program and study level meetings, as applicable, and provides relevant updates to SSE team members.
- Attends kick-off meetings, investigator meetings (in region)
- Development of Strategic Site Relationships
- The Sr. Manager, Study Site Engagement, may be responsible for developing and maintaining long-term strategic relationships with selected sites/site networks to improve the site and Takeda experience.
- Conferences, Congresses, Other Site Facing Events
- The Sr. Manager, Study Site Engagement may be tasked to help the Associate Director, Study Site Engagement with developing and executing the SSE strategy for non-study specific activities within their designated Therapeutic Area (TA) or Country.
- Through participation in conferences or congresses, the Sr. Manager, Study Site Engagement utilizes these key site-facing events to connect with sites beyond their physical locations.
- This role involves engaging with new clinical trial investigators or those unfamiliar with Takeda, thereby promoting support for the advancement of our pipeline.
CORE ELEMENTS RELATED TO THIS ROLE
Technical/Functional (Line) Expertise
- Understanding of clinical trials and advanced knowledge of ICH-GCP, Clinical trials regulations, and applicable global and regional/country requirements.
Decision-making and Autonomy
- Able to make sound decisions after identification of an issue and being able to make careful consideration of various courses of action towards resolution.
- Considers the short and long-term impact of those decisions in terms of risk to Takeda from a regulatory, legal, financial and business acumen perspective.
Influencing and motivational skills
- Needed for tactful and business smart communication with key internal- and external stakeholders.
Interaction
- The Senior Manager, Study Site Engagement regularly interacts with internal and external stakeholders. Key stakeholders for this role include but are not limited to Takeda Clinical Operations, Takeda Clinical Study Start-up and Engagement (CSSE) functions, Takeda Clinical Science, Takeda Medical Affairs, local R&D functions, site and CRO personnel.
Innovation
- Foster enhanced site engagement by executing the global engagement strategy. Utilize innovative thinking to overcome obstacles and achieve goals.
Complexity
- Possesses inter-cultural competencies and ability to work cross-functionally in a complex global organization.
Education, Behavioural Competencies and Skills
Education:
- Bachelor's Degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences or drug development is required.
- A clinical or advanced degree (BSN, MS, MA, MBA, PharmD) is preferred.
Experience:
- 7+ years of experience in clinical research, either with a CRO or a pharmaceutical company, focusing on clinical trials.
- Experience may also include roles such as Study Coordinator or Study Nurse, where close collaboration with Clinical Research Associates was involved.
- While experience in a Lead CRA or managerial role is preferred, it is not mandatory.
- The total cumulative work experience of the candidate may also be taken into consideration.
- Extensive site management and/or monitoring experience across a range of highly complex disease areas.
- Demonstrated capability of effective site oversight.
- Solid knowledge of clinical development processes with strong emphasis on site management.
- Ability to lead, troubleshoot and influence for quality and delivery.
- Proven experience in effectively communicating with site staff including KOLs.
- Experience in all study phases and in multiple indications preferred.
- Comprehensive and current regulatory knowledge, including GCPs.
Essential Qualifications
- Extensive site management and/or monitoring experience across a range of highly complex disease areas.
- Demonstrated capability of effective site oversight.
- Solid knowledge of clinical development processes with strong emphasis on site management.
- Ability to lead, troubleshoot and influence for quality and delivery.
- Proven experience in effectively communicating with site staff including KOLs.
- Experience in all study phases and in multiple indications preferred.
- Comprehensive and current regulatory knowledge, including GCPs.
Additional Skills
- Good organizational skills and ability to deal with competing priorities.
- Effective communication skills (written, verbal in English and local language).
- Good creative thinker, curious and unafraid to ask questions.
- Innovator, willing to initiate changes, introduce new ideas, and creatively problem solve.
- Proficient with MS Office Suite (Excel, Word and PowerPoint).
Additional Information
Demonstrates flexibility in schedule and willingness to travel frequently (at least 30% and as high as 50% during busy periods).
Locations
POL - Poland
Remote Base Salary Range
żł313,200.00 - żł430,650.00
Benefits
For information about our benefits, please click here.