Alliance and Scientific Senior Specialist/Manager

at  Autolus Ltd

London, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Nov, 2024Not Specified22 Aug, 2024N/AGood communication skillsNoNo
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Description:

Responsibilities:

ROLE SUMMARY

The alliance and scientific lead will be responsible for managing the relationship with and activities provided by 3rd party partners/vendors of the Translational Medicine department. Internally, they will work in a cross-functional setting, collaborating with multiple teams within the company, including clinical operations, clinical development, biometrics, etc. They will build strong working relationships both with internal stakeholders and our external 3rd party vendors. They will ensure alignment with company priorities, meet internal deadlines and clinical study requirements. They will contribute their scientific expertise during vendor selection, development and validation of new assays where required and ongoing vendor oversight. They will provide detailed oversight of vendor activities ensuring the delivery of high-quality services and data to support ongoing clinical trials.

KEY RESPONSIBILITIES

  • Be a key member of the clinical study team to understand and align testing needs with clinical, regulatory and commercial requirements.
  • Contribute to authoring/amending clinical study documents.
  • Liaise with members of the Clinical Development and Clinical Operations teams to understand the requirements for sample collection and logistics.
  • Identification of potential assay development needs and the requirement for outsourcing.
  • Investigate assessment availability and quality at 3rd party vendors, perform official vendor selection, due diligence and onboarding of new vendors
  • Contribute to contract negotiations, master service agreements, statements of work and analytical plan authoring.
  • Provide budget plans, updates and efficient tracking of costings.
  • Provide day-to-day oversight of vendor activities, tracking KPIs and contributing to the creation and management of vendor oversight plans.
  • Ensure the prompt and efficient assessment of clinical patient samples, identifying ways and means to optimise processes/workflows.
  • Support the planning, on-time delivery and accurate interpretation of high-quality data to be used for publications and regulatory submissions.
  • Collaborate cross-functionally with multiple teams (procurement, product development, business development, R&D, regulatory, quality, global development) to establish new relationships/strengthen current working relationships and contribute to company-wide goals.
  • Be the Alliance and Scientific Management (ASM) lead for outsourced activities for specific clinical studies within the Translational Medicine team.
  • Identify, document and implement new processes within the team
  • The post-holder will work with 3rd party laboratories who will generate data using our samples. You will contribute your scientific expertise to both ensure services are provided to a high-quality standard and the generation of bespoke assays are developed to our requirements.
  • This role is primarily computer-based and would request the successful candidate to attend the Mediaworks office at least once per week.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

London, United Kingdom