Proj Mgr Clin Supplies

Great opportunity to join our Global Clinical Supplies team, in a Project Manager role!

Responsible for providing overall global coordination of the entire clinical supplies life-cycle for the projects assigned. 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. Provides consultation services to clients regarding global packaging, labeling, and distribution requirements. Serves as the main point of contact between the client, clinical project teams, third party vendors, and study sites.

Great opportunity to join our Global Clinical Supplies team, in a Project Manager role!

Responsible for providing overall global coordination of the entire clinical supplies life-cycle for the projects assigned. 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. Provides consultation services to clients regarding global packaging, labeling, and distribution requirements. 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 interactionsSound understanding of global clinical supply label requirements and regulationsExperienced in protocol interpretation and packaging and labeling design cGMP, GCP, and ICH knowledge and experience essential

Knowledge, Skills and Abilities:Familiar with the global drug development processesUnderstanding of drug formulation, analytical method development, stability, and bulk drug manufacturing practicesExperienced in clinical supplies packaging and labeling designKnowledge and experience in managing third party clinical supplies packaging and labeling facilitiesStrong knowledge of the complete clinical supplies life cycleSkilled in client relationship managementVery strong communication skills both written and verbalExcellent interpersonal skills and problem solving/decision making skillsDemonstrate effective leadership and team building skills

Strong computer skills:

Working knowledge of Microsoft Project, Excel, and Microsoft Word is requiredStrong organizational skills requiredStrong multi tasking skills required

PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities.

PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary for typical working hours.

Ability to use and learn standard office equipment and technology with proficiency.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

May require travel. (Recruiter will provide more details).

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 interactionsSound understanding of global clinical supply label requirements and regulationsExperienced in protocol interpretation and packaging and labeling design cGMP, GCP, and ICH knowledge and experience essential

Knowledge, Skills and Abilities:Familiar with the global drug development processesUnderstanding of drug formulation, analytical method development, stability, and bulk drug manufacturing practicesExperienced in clinical supplies packaging and labeling designKnowledge and experience in managing third party clinical supplies packaging and labeling facilitiesStrong knowledge of the complete clinical supplies life cycleSkilled in client relationship managementVery strong communication skills both written and verbalExcellent interpersonal skills and problem solving/decision making skillsDemonstrate effective leadership and team building skills

Strong computer skills:

Working knowledge of Microsoft Project, Excel, and Microsoft Word is requiredStrong organizational skills requiredStrong multi tasking skills required

PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities.

PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary for typical working hours.

Ability to use and learn standard office equipment and technology with proficiency.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

May require travel. (Recruiter will provide more details).