Clinical Trial Coordinator - Munich, Deutschland - Thermo Fisher Scientific

Thermo Fisher Scientific

Geprüftes Unternehmen

Munich, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Clinical Trial Coordinator - Client Dedicated - Munich

Who is PPD Clinical Research Services?

PPD is a leading global contract research organization. Our purpose is to improve health. Our mission is to help customers deliver life-changing therapies. Our strategy is to bend the cost and time curve of drug development and optimize value for our customers. PPD is now part of Thermo Fisher Scientific.

As the world leader in serving science, our Mission is to enable our customers to make the world healthier, cleaner and safer.

We are excited about the opportunities this combination brings to enhance our comprehensive end-to-end offering, enabling customers to move rapidly from scientific idea to approved medicine

The PPD FSP Solution:

PPD's Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions.

We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality.

We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.

Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.

Responsibilities:

Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
Reviews regulatory documents for proper content
Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
Assists with the identification of potential investigators and development/distribution of initial protocol packets
Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes

Education and Experience:

University degree, or equivalent in education, training and experience
Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all nonclinical/clinical aspects of project implementation, execution, and closeout
Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
Experience of managing multiple projects with differing priorities at one given time
Exceptional communication, collaboration, organisational and time management skills.
Fluency in English and German, at least to C1 level

At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team.

We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential.

Our 4i values:

Integrity
Innovation
Intensity
Involvement

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Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us.

As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.

#StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access:

- "Severely disabled applicants with the same aptitude will be given preferential treatment. / Schwerbehinderte Bewerber werden bei gleicher Eignung bevorzugt behandelt."_