Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

The Planet Group

Clinical Labeling Operations (Project Coordinator)

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
73
out of 100
Average of individual scores

Were these scores useful?

Job Description

Job:
Clinical Labeling Operations (Project Coordinator)
Pay:
$53.96/hr - $53.96/hr
Duration:
12 months
Location:
Full list of preferred locations (ranked in order of preference) is within 50 miles of: 1. Thousand Oaks, CA 2. El Segundo, CA 3. Frederick, MD 4. Oceanside, CA 5.
Foster City, CA Essential Functions:
Responsible for the coordination of new clinical labeling implementation with Regulatory Affairs Labeling, Quality Assurance Labeling, Supply Chaing Labeling BPO, PM's and multiple packaging sites worldwide. Creates labels content and maps content to the appropriate fields in Bartender Creates Business Continuity Labels and maps contents to the appropriate fields Reviews clinical final product label content and Bartender mapping to ensure all content matches source documents and text is mapped to the appropriate fields. Liaises with Regulatory Affairs Labeling colleagues to obtain correct text, negotiate timelines and ensure that all requirements have been met. Manages the completion of operational excellence projects where prior precedents may not be set and outcomes require executing without prior experience. Authors standard operating procedures, guidelines and work instructions. Collaborates with team members to meet departmental goals and objectives. Completes labeling updates as assigned.
Knowledge, Experience and Skills:
Highly capable at directing and coordinating project work. Strong verbal, technical writing and interpersonal skills. Proficient in Microsoft Office applications. Knowledge of FDA and cGMP standards as well as regulatory guidance documents. Prior experience in pharmaceutical or other regulated industry is required. Prior experience in clinical or commercial supply chain Familiarity with artwork/labeling production. Familiarity with Bartender software is bonus. 6+ years of relevant experience and a BS or BA or 4+ years of relevant experience and a MS.