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Adaptimmune Therapeutics

https://www.adaptimmune.com/

Current Openings

Vice President, Business Development
The VP, Business development will work alongside the Chief Business Officer as a key leader within the Business Development and Alliance Management Team. This position will focus on the pursuit of strategic business development and M&A opportunities, partnerships, alliances and licensing agreements that fit within the overall corporate strategy, business plan and product portfolio.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Business Development
25 days ago days ago
Associate Director, Clinical Translational Lead
This is a senior role in the Translational Sciences team which functions out of both our UK and USA sites, providing broad translational sciences support to Adaptimmune’s clinical programs, and to the research teams.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Clinical Research
11 months ago days ago
Associate Director, Global Regulatory Affairs - CMC (hybrid)
We are seeking a highly motivated and experienced individual for an Associate Director position in global Regulatory Affairs CMC. This position will provide CMC regulatory leadership and act as the point of contact on cross-function teams to support the strategy and development of our T cell therapies for the treatment of cancer.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Regulatory Affairs
11 months ago days ago
Senior/Principal Bioinformatician
This role is a senior functional team member supporting Bioinformatics activities on assigned Research (e.g., Translational Sciences, Allogeneic), Enterprise Data & Analytics, and QDS projects, including contributions to milestone planning and delivery, data and knowledge stewardship, and internal and external publications and presentations.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Biostatistics
11 months ago days ago
Senior Director Corporate Compliance
The role will include (but is not limited to): managing the teams, setting and developing policies, managing training, overseeing and implementing compliance requirements, working with compliance vendors, monitoring and managing the privacy reporting obligations, policies and processes, managing the EH&S teams globally.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Quality
11 months ago days ago
Clinical Quality and Compliance Specialist
The purpose of the Clinical Quality and Compliance (CQC) Specialist role is to conduct a broad range of activities that support the CQC department and its sub-groups (Trial Master File (TMF) Compliance, Clinical Compliance, and Clinical Quality) to fulfil their objectives.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Quality
11 months ago days ago
Clinical Scientist-Associate Director
The Clinical Scientist will be responsible for global clinical trial delivery including the planning, management and reporting of trials in accordance with company plans/objectives, GCP, local country requirements and company standard operating procedures.
Annually: USD 0 - 0
Full Time
On-Site/Hybrid
Clinical Research
11 months ago days ago

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