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About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
For more information, please visit www.thermofisher.com.
Provides complete oversight of supply chain for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. Acts as a representative for the department on all assigned projects
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.
Represents the department internally and externally at meetings, strategic
projects and initiatives as per the business requirements.
Mentors and guides supports junior team members.
Participates in process improvement initiatives.
Maintains and uses existing tools while continously looking for improvement
opportunities.
May participate in the bidding and/or bid defense opportunities client contact for their supply chain requests/questions/concerns.
Education and Experience:
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
5+ years).
Required profile
Experience
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.
Clinical Trial Manager/Project Manager II - MUST have Post Trial Access (PTA) / Expanded access program (EAP) Fully remote - Bulgaria/Spain/Italy/Poland/Canada
Clinical Trial Manager/Project Manager II - MUST have Post Trial Access (PTA) / Expanded access program (EAP) Fully remote - Bulgaria/Spain/Italy/Poland/Canada