Job Description
Are you passionate about making a difference in the world of healthcare? Do you want to be part of a dynamic team dedicated to transforming lives through innovative therapies? Join us and be a key player in shaping the future of medicine!
We are a leading company at the forefront of gene editing and advanced therapeutics, with a diverse portfolio of groundbreaking treatments. We're committed to revolutionizing the way we approach healthcare and are looking for exceptional individuals to help us achieve our mission.
Your Role:
As the Associate Director of Clinical Supply Chain Planning, you'll be a vital part of our team, ensuring that clinical supplies are available on time and in the right quantities to support our exciting clinical trials. You'll be responsible for crafting and optimizing supply plans, collaborating with various stakeholders, and driving operational excellence.
Key Responsibilities:
Clinical Supply Planning: Develop and manage clinical supply plans to support manufacturing, labeling, and forecasting activities across multiple programs.
Demand Forecasting: Work closely with clinical teams and stakeholders to forecast demand based on trial protocols and timelines.
Coordination: Ensure seamless coordination with manufacturing sites, clinical sites, and vendors to maintain consistent inventory levels throughout the supply chain.
Packaging and Labeling: Oversee packaging and labeling operations, both internally and with external partners, to meet clinical supply requirements.
KPI Implementation: Define and track KPIs and metrics related to supply and demand to measure performance and drive improvements.
Issue Resolution: Identify and address potential issues or risks related to clinical supply, providing solutions to meet timelines.
Process Improvement: Continuously evaluate and enhance supply chain planning processes to optimize efficiency.
Compliance: Adhere to established SOPs and GXP requirements to ensure high-quality operations.
What We're Looking For:
Education: Bachelor's degree in Biological Sciences or a related field.
Experience: 10-12+ years of experience in a cGMP supply chain environment, with a strong understanding of GCP regulations.
Skills: Proficiency in Microsoft Office (Word, Excel, Outlook) and experience with clinical supply chain planning.
Attributes: Exceptional organizational skills, attention to detail, and the ability to thrive in a fast-paced, ever-changing environment.
Communication: Clear and effective verbal and written communication skills.
Analytical Skills: Strong problem-solving and critical thinking abilities, with the capability to influence others and work collaboratively.
Preferred Qualifications:
Experience with cold chain logistics and cell/gene therapies.
Professional certifications such as APICS CPIM or CSCP.
Excellent interpersonal skills and the ability to build strong relationships with internal and external partners.
Why Join Us?
We believe in creating a collaborative and supportive work environment that combines the flexibility of remote work with the benefits of in-person interactions. You'll have the chance to work closely with a talented team, contribute to groundbreaking projects, and grow both professionally and personally.
Commitment to Diversity:
We are dedicated to creating an inclusive workplace where all employees feel valued and respected. We encourage candidates from all backgrounds to apply.
If you're ready to take on an exciting challenge and be part of a team that's making a real impact, we'd love to hear from you!
Employment Type: Full-Time
Salary: $ 197,800.00 Per Year
Job Tags
Full time, Remote job,