Project Mgr/senior Project Mgr, Global Clinical

hace 7 meses

Ciudad de México Thermo Fisher Scientific A tiempo completo

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 cover 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 responsibilities**:
A 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 labelling 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, labelling, 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 labelling design
- GMP, GCP, and ICH knowledge and experience essential

**Knowledge, Skills and Abilities**:

- 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 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.

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 value 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 organisation but with a local feel.
- We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing -We are one PPD

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