Sr Project Manager, Clinical Supplies - FSP - EMEA

IT-Systemhaus der Bundesagentur für Arbeit; Deutschland; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading clinical research organization is seeking a Sr Project Manager for Clinical Supplies. This role involves overseeing supply chains for complex global clinical trials and ensuring compliance with company requirements. The ideal candidate will possess a bachelor's degree and over 8 years of relevant experience, along with strong communication and leadership skills. Join a mission-driven team dedicated to making the world healthier, cleaner, and safer.

Qualifikationen

• 8+ years of relevant experience in project management.
• Ability to work independently with little guidance.

Aufgaben

• Oversee supply chain for global clinical trials.
• Develop study specific plans for each project.
• Integrate clinical supplies into the supply chain.
• Consult clients on clinical trial management.

Kenntnisse

Strong English and communication skills both written and verbal

Strong interpersonal, planning, organizational skills

Effective leadership and team building skills

Strong focus on customers and attention to detail

Good understanding of clinical supply operations

Ausbildung

Bachelor's degree or equivalent

Tools

Microsoft Office suite

Jobbeschreibung

Sr Project Manager, Clinical Supplies - FSP - EMEA

Sr Project Manager, Clinical Supplies - FSP - EMEA

Beginn

• Projektassistent/in

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

This role will be embedded within a client dedicated team. You will work alongside the clients own experienced personnel, as well as PPD colleagues to deliver innovative clinical support to non interventional studies.

Discover Impactful Work:

You will provide complete oversight of supply chain for complex global clinical trials. Ensuring project/study activities are in compliance with company and client requirements. Acts as a representative for the department on all assigned projects.

A day in the Life:

• Develops study specific plans for each assigned project.
• Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
• Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
• Participates in ongoing training on new regulations.
• May participate in aspects of the bidding process.
• Represents the department internally and externally at meetings, strategic
  projects, bid defense meetings and initiatives as per the business requirements
• Pro-actively works on process improvement initiatives.
• Maintains and uses existing tools while continously looking for improvement
  opportunities.
• Consults the client on the best strategy for management of the clinical trial.
• Builds strong internal and external network.

Education:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).

Knowledge, Skills, Abilities

• Strong English and communication skills both written and verbal
• Strong interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills
• Effective leadership and team building skills
• Strong working knowledge of Microsoft Office suite
• Strong focus on customers and attention to detail
• Ability to work in team environment, as well as work independently with little guidance
• Good understanding of clinical supply operations
• Solid client building and 3rd party relationship management
• Ability to provide customer service with the highest standards of quality and excellence

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 color, religion, ___ orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.