Associate Director, Study Site Engagement
vor 2 Wochen
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.
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Job DescriptionAre 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 reporting to the Director, Study Site Engagement based in Australia.
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 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: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 feasibilitySupports 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 initiationSupports 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 phaseSupports 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.TrainingApplicable local regulationsSOP trainings (Takeda and CRO, as applicable)TA/Study specific trainingNon-Study Specific Engagement activities:People ManagementThe 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 roleEstablishes 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 programsThe 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 RelationshipsThe 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 EventsThe 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) 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.LocationsAUS - Australia Remote
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
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