Gma, Gme Operations, Study Implementation Lead

vor 3 Monaten

Zürich ZH, Schweiz Takeda Pharmaceutical Vollzeit

Our team is growing and for this we need bright minds with creativity and flexibility - **what talent do you have?**

**Role Objectives**
- Accountable for overseeing EUCAN RWE Medical Affairs Company Sponsored (MACS) study preparation in different Therapeutic Areas for both in line and pipeline products with the support of the relevant Evidence Generation Lead and Medical Lead/Head
- Accountable for supporting internal submissions, Feasibility Assessments and study activations of EUCAN RWE MACS studies
- Accountable for overseeing EUCAN RWE Study Execution and study plans (including Study Management Plan and Risk Assessment Plan)
- Responsible for engaging with external vendors/CROs at selection/contracting and for overseeing vendors/CRO activities through the end of the study
- Responsible for maintaining and overseeing the TMF until study close-out and reporting
- Responsible for the conduct of studies in accordance with all applicable internal legal and compliance policies (SOPs) as well as applicable regional or country specific regulatory guidelines

**Accountabilities**
- Support the preparation of study synopsis and study protocol of EUCAN RWE studies in different Therapeutic Areas with the support of the relevant Evidence Generation Lead and Medical Lead
- Prepare RFPs, detailed timelines and budget and establish a contract / SOW with selected CRO
- Support/manage initial submissions and manage study start-up, activation, implementation, execution, study close-out and reporting activities, including overseeing study related documentation and plans (e.g. Study Management Plan, Risk Assessment Plan, etc.)
- Participate in Steering Committee Meetings and provide regular updates on study progress
- Maintain and oversee the TMF and relevant study repositories until study closure / reporting
- Support LOC study implementation and study execution in accordance with Takeda policies and procedures

**Key Capabilities**
- Knowledge in outcomes, Real-World Evidence studies and Epidemiologic research
- Project Management experience with a proven track record in study start-up and execution
- In-depth knowledge of GCP, GVP and GPP
- Advanced knowledge of the pharmaceutical industry, including experience with data generation within life-cycle development and knowledge of clinical studies and associated documents and systems
- Extensive knowledge of regulations and industry standards applicable to RWE studies
- Vendor management experience
- Experience managing study management systems and study document repositories

**Education, behavioral competences and skills**
- Minimum MSc degree (preferably PhD), preferably in a health sciences related field with 8 years of research related experience and/or pharmaceutical industry experience (including CRO)
- Strong written and verbal communication skills (English)

**Empowering our people to shine**

At Takeda, we earn the trust of society and our customers through our values of Takeda-ism: Integrity, Fairness, Honesty, Perseverance. We incorporate these values in everything we do. They represent who we are and how we act. They help us make decisions that we can be proud of today and in the future. We enable our employees to develop their full potential. As a global top employer, we offer exciting career paths, promote innovation, and strive for top performance in everything we do. Takeda fosters an inclusive, collaborative, and international work environment where our teams are united by their relentless commitment to our goal of improving people's health and creating a better future for the world.

**Diversity, Equality, and Inclusion**

Takeda is committed to foster diversity, equality, and inclusion. Hiring decisions are based entirely on qualifications and are made regardless of gender, ethnic origin, religion, sexual orientation, age, or disability.

**Locations**:
Zurich, Switzerland

**Worker Type**:
Employee

**Worker Sub-Type**:
Regular

**Time Type**:
Full time

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