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Project Mgr/senior Project Mgr, Global Clinical
hace 4 semanas
Thermo Fisher Scientific
We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.
Our Global Clinical Supplies team covers all aspects from purchasing to global inventory management and from distribution to destruction. We have a new vacancy for Project Manager/Senior Project Manager (depending on experience) for our Global Clinical Supplies team to be based in the LATAM region. This can be office-based or home-based.
Key ResponsibilitiesA Project Manager (PM) in the GCS team is responsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. Also responsible for managing the more complex clinical supplies studies. These studies require primary and/or secondary packaging and labeling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project-specific material for multiple projects at the same time. The PM provides consultation services to clients regarding global packaging, labeling, and distribution requirements. This person also serves as the main point of contact between the client, clinical project teams, third-party vendors, and study sites.
Education and Experience- Bachelor's degree in a science or related discipline
- 3-5 years in clinical research industry, specifically in the area of Clinical Supplies, Clinical Development, QA/Regulatory Affairs
- Skilled in client and internal team interactions
- Sound understanding of global clinical supply label requirements and regulations
- Experienced in protocol interpretation and packaging and labeling design
- GMP, GCP, and ICH knowledge and experience essential
- Familiar with the global drug development processes
- Understanding of drug formulation, analytical method development, stability, and bulk drug manufacturing practices
- Experienced in clinical supplies packaging and labeling design
- Knowledge and experience in managing third-party clinical supplies packaging and labeling facilities
- Strong knowledge of the complete clinical supplies life cycle
- Skilled in client relationship management
- Very strong communication skills both written and verbal
- Excellent interpersonal skills and problem-solving/decision-making skills
- Demonstrate effective leadership and team-building skills
- Strong computer skills: working knowledge of Microsoft Project, Excel, and Microsoft Word is required
- Strong organizational skills required
At PPD we hire the best, develop ourselves and each other, and recognize 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. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly values a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
- We have a strong will to win
- We earn our customer's trust
- We are game changers
- We do the right thing
- We are one PPD
