Associate Director, Study Site Engagement

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 Takedas and I further attest that all information I submit in my employment application is true to the best of my knowledge Are you looking for a patient-focused company to inspire you and support your career If so be empowered to take charge of your future at Takeda Join us as an Associate Director Study Site Engagement based in India This position is field based with monthly visits to the Takeda Delhi Mumbai office 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 towards for excellence in everything we do We foster an inclusive collaborative workplace in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world Here you will be a vital contributor to our inspiring bold mission GOALS Covering India and other countries in the region the Associate Director 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 The Associate Director Study Site Engagement establishes communication with regional country Medical Affairs MA provides updates on study site status and establishes site engagement study specific strategies Associate Director Study Site Engagement supports study teams with trial operations from Feasibility through CSR within the assigned region or countries across Takeda therapeutic areas The Associate Director Study Site Engagement enhances engagement and offers added value by providing guidance and sharing knowledge with study sites while establishing and nurturing long-term relationships with investigators and study site personnel The Associate Director Study Site Engagement supports country and site identification feasibility site selection study recruitment strategies and mitigates barriers at the direction of Clinical Programs The Associate Director Study Site Engagement supports Takeda study teams as part of their day-to-day responsibilities and may act as an SSE-Program Lead SSE-PL and or SSE-Study Lead SSE-SL ACCOUNTABILITIES Study Specific Engagement activities Early engagement - Country and site feasibility Supports the 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 SSE LOC support Reports any discrepancy on feasibility progress to SSE-PL SSE-SL 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 of 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 Enrollment and study conduct phase Supports recruitment strategy and activities when targets are not met e g utilization of PR R materials booster visits phone contacts Interacts closely with local CRO team throughout the lifecycle of the study Helps coordinate and or attend booster visits or other activities requested by SSE-PL SSE-SL Regularly interacts with priority sites in assigned trials Training Applicable local regulations SOP trainings Takeda and CRO as applicable Therapeutic Area Study specific training Non-Study Specific Engagement activities participation in following activities may vary depending on assignment by line manager People Management The Associate Director Study Site Engagement may be responsible for resource and talent management of Sr Managers and or Managers SSE as applicable across relevant regional country clusters to achieve site engagement deliverables and GDO objectives Cross-functional role Establishes communication and regular interactions with regional country Medical Affairs MA and provides updates on planned and ongoing global clinical studies with a focus on country landscaping upcoming feasibilities study status and enrollment updates specific site issues and HCPs contacted in the region country SSE Program Lead and or SSE Study Lead for assigned programs The Associate Director of Study Site Engagement plays a key role in shaping 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 Associate Director 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 Associate Director of Study Site Engagement may be tasked 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 Associate Director of 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 EDUCATION EXPERIENCE Scientific degree MD PhD MA MS BA BS with preference for MD or PhD in pharmaceutical science chemistry biology medical healthcare is preferred but not mandatory 10 years of experience in clinical research either with a CRO or a pharmaceutical company focusing on clinical trials The total cumulative work experience of the candidate may also be taken into consideration Ability to work independently and in teams Work cross-functional globally Clinical trials processes Clinical trials regulations as per regional country requirements Advanced knowledge and understanding of ICH-GCP Healthcare industry knowledge preferred Outsourcing CRO knowledgebase Common computer programs and databases such as MS Office Global and cross boundary communication Relationship Management Influencing skills Fluent in spoken written English Travel Travel frequently in assigned region required travel may be as high as 40 during busy period Locations Mumbai IndiaWorker Type EmployeeWorker Sub-Type RegularTime Type Full time