Clinical Trial Supply (CTS) Study Manager

Posted Yesterday
Be an Early Applicant
41 Locations
Remote
Senior level
Biotech
The Role
Plan and manage clinical trial supplies for low-to-medium complexity studies: forecast drug volumes, collect/analyze samples, ensure storage/transport/archiving, manage vendors, use IRT, author/review study documents, lead global CTS meetings, partner with R&D, and update SOPs for continuous improvement and compliance.
Summary Generated by Built In

Work Environment:

*** This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly.  Relocation and mobility assistance are not provided.

Main Responsibilities:

  • Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies

  • Performs planning and forecasting of drug volume requirements

  • Sample collection and analysis

  • Ensures proper storage, transportation and archiving

  • Assists with selection and management of external service providers in compliance with outsourcing strategy to ensure cost efficient and high quality services

  • Leverages interactive response technology (IRT) system to support clinical supply management activities

  • Authors/reviews critical study documents (e.g. study protocol, product dossiers, handling instructions, study reports)

  • Leads or participates in global Clinical Trial Supply project meetings with internal and external team members

  • Partners with R&D and other functions to ensure optimal use of systems and processes to support clinical trial supply chain

  • Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities

Minimum Qualifications:

  • Bachelors Degree in Life Sciences, Engineering, Logistics or equivalent experience

  • 5+ years of experience in clinical supply management with the pharmaceutical industry

  • Demonstrated knowledge of ICH-GCP regulations and the conduct of clinical studies

  • Demonstrated knowledge of cGMP and cGDP regulations

  • Team-player with proven effective interpersonal and communication skills

About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor  visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

 

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.


You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

 To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

 

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Skills Required

  • Bachelor's Degree in Life Sciences, Engineering, Logistics or equivalent experience
  • 5+ years of experience in clinical supply management with the pharmaceutical industry
  • Demonstrated knowledge of ICH-GCP regulations and the conduct of clinical studies
  • Demonstrated knowledge of cGMP and cGDP regulations
  • Experience leveraging Interactive Response Technology (IRT) systems to support clinical supply management
  • Proven effective interpersonal and communication skills; team-player
  • Hybrid role with a minimum of 3 days onsite weekly (relocation/mobility assistance not provided)
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The Company
HQ: Melbourne, Victoria
20,401 Employees

What We Do

CSL is a leading global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL – including our businesses, CSL Behring, CSL Seqirus, CSL Plasma and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. See our community guidelines: https://bit.ly/3Bs17Ra

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