Study coordinator Jobs in Affoltern Am Albis

Description

At our heart we are committed colleagues. We offer interested people numerous opportunities and strongly believe in, and promote, diversity, equity, and inclusion. As a company we offer roles based on merit, welcoming candidates of any gender, age, religious belief, sexual orientation, race, color, ethnic or social origin, or disability.

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.

If you are interested in this opportunity, we look forward to receiving your application via our online tool!

Learn more at

Locations

Zurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time