Assoc Proj Mgr Clin Supplies

Wonderful entry level opening that will allow you to get into industry, and into Global Clinical Supplies as a project manager!

Manages clinical supply activities in support of the company's ongoing global clinical trials. Assists senior Global Supply Managers in these activities, and may perform the function on the least complex and least difficult studies (i.e., ancillary supplies (no drug) or distribution of study drug and supplies). May represent GCS to the project team for projects in which they are assigned.

Wonderful entry level opening that will allow you to get into industry, and into Global Clinical Supplies as a project manager!

Manages clinical supply activities in support of the company's ongoing global clinical trials. Assists senior Global Supply Managers in these activities, and may perform the function on the least complex and least difficult studies (i.e., ancillary supplies (no drug) or distribution of study drug and supplies). May represent GCS to the project team for projects in which they are assigned.Education and Experience:Bachelor's degree in a science or related discipline1-3 years in clinical research industry, specifically in the area of Clinical Supplies, Clinical Development, QA/Regulatory Affairs.

Familiar with clinical supply terminology and practices and principles.

Familiar with protocol interpretation and packaging and labeling design

Familiar with cGMP, GCP, GDP, and ICH knowledge and experience essential

Knowledge, Skills and Abilities: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.

Strong multi tasking skills required.

Education and Experience:Bachelor's degree in a science or related discipline1-3 years in clinical research industry, specifically in the area of Clinical Supplies, Clinical Development, QA/Regulatory Affairs.

Familiar with clinical supply terminology and practices and principles.

Familiar with protocol interpretation and packaging and labeling design

Familiar with cGMP, GCP, GDP, and ICH knowledge and experience essential

Knowledge, Skills and Abilities: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.

Strong multi tasking skills required.