Job Openings
Remote Scientific Project Manager | Biosimilar Programs
About the job Remote Scientific Project Manager | Biosimilar Programs
Job Title: Remote Scientific Project Manager | Biosimilar Programs
Job Location: Thousand Oaks, CA, USA
Job Location Type: Remote
Job Contract Type: Contract
Job Seniority Level: Entry level
Job Overview
We are seeking an accomplished Scientific Project Manager to play a crucial role in advancing our biosimilar programs through the commercialization process. This fully remote opportunity is designed for individuals who thrive in both independent and collaborative environments, contributing to a dedicated team committed to the success of biosimilar candidates. As a key figure in managing workflows, you will work alongside technical teams and oversee sample management to facilitate regulatory approvals.
Key Responsibilities
This position offers a meaningful opportunity to significantly impact biosimilar development while fostering an environment that supports your professional growth and advancement as you acquire valuable project management and scientific skills.
Employment Type: Contractor
We are seeking an accomplished Scientific Project Manager to play a crucial role in advancing our biosimilar programs through the commercialization process. This fully remote opportunity is designed for individuals who thrive in both independent and collaborative environments, contributing to a dedicated team committed to the success of biosimilar candidates. As a key figure in managing workflows, you will work alongside technical teams and oversee sample management to facilitate regulatory approvals.
Key Responsibilities
- Provide project management expertise to support the biosimilar business unit’s sample management and project workflows, collaborating effectively with cross-functional teams to enhance operational processes.
- Engage closely with the Similarity Team, Critical Reagents Group (CRG), Data Management, and other scientific personnel to strategically plan and uphold inventory.
- Manage the logistics of sample distribution for testing and convey test results within the biosimilar project teams.
- Develop electronic laboratory notebooks (ELN) for sample submissions, generating lot numbers and sample IDs, while retrieving data utilizing Quality Control Laboratory Information Management Systems (QC LIMS).
- Assist colleagues with ELN software usage, updating work orders, and supporting database queries, including data retrieval, organization, and verification.
- Archive documents in the controlled document repository and conduct data verification for internal documentation and regulatory submissions.
- Utilize your scientific expertise to meticulously review regulatory documents, ensuring accuracy and compliance with established protocols.
- Format documents to meet internal guidelines, ensuring uniformity and compliance across all documentation.
- Exceptional communication abilities and a keen eye for detail.
- A solid scientific background with a degree in a relevant scientific field (laboratory experience is a plus).
- Proficiency in Microsoft Excel and Word.
- A proactive approach to working independently following training.
- Superior time management skills with experience in data handling.
- Doctorate degree; OR
- Masters degree with a minimum of 2 years of relevant experience; OR
- Bachelors degree with at least 4 years of relevant experience; OR
- Associate degree with 10+ years of relevant experience; OR
- High school diploma/GED with 12+ years of relevant experience.
This position offers a meaningful opportunity to significantly impact biosimilar development while fostering an environment that supports your professional growth and advancement as you acquire valuable project management and scientific skills.
Employment Type: Contractor
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