Job type
PermanentLocation
London / remoteWorking Pattern
Flexible Working,Full-timeSpecialism
Clinical Data ManagementIndustry
PharmaceuticalsPay
£100-140,000 plus bonus & package
Senior Director, Clinical Trial technology process, QA & regulatory compliance, London/hybrid/remote biotech
Your new company
They are looking to add a Director / Senior Director of Process and Compliance to help them move the company’s Clinical Technologies forward and are offering an excellent package plus significant remote working flexibility and the chance to make a real impact.
Your new role
What you'll need to succeed
Experience of rare disease / small cohort trials would be an advantage, but is not necessary for this role.
What you'll get in return
What you need to do now
Keywords: clinical, data, management, manager, quality, systems, process, compliance, controls, tools, CSV, validation, regulatory, compliance, computer, systems, SDTM, ADAM, CDISC, SAS, Snowflake, QA, audit, 21-CFR Part 11, Director, VP, drug, development, R&D, discovery, IT, pharmaceutical, biotech, operations
Hays have been exclusively retained by an extremely well-funded biotech driving breakthrough innovations in the space of gene therapy.
They have developed an innovative new technology that allows them to deliver gene therapies in a novel way to patients with rare diseases and are currently going into their initial clinical trial to validate its use. Alongside this they have multiple other programmes approaching the clinic and several more in development, giving them a very strong pipeline.
The company prides itself on innovation and collaborative work and has a very experienced senior leadership & technical team coupled with a C-suite with a truly impressive track record.
Your new role
This is a permanent position, working closely with the CEO, VP Biometrics and other senior stakeholders to ensure clinical (and potentially other, earlier discovery) technologies remain compliant with regulatory requirements as well as driving innovation within this space, eg through the adoption of new processes/technologies/software, etc.
The company is ideally looking for candidates to spend some time in office, but the exact amount is open for discussion dependent on candidate location and other factors.
Major responsibilities will include a mix of (but aren’t limited to):
- Establish the implementation roadmap for all clinical technologies that enable clinical trial management and data collection mechanisms
- Develop, manage and implement processes for clinical technology adoption and management, eg software solutions
- Drive new technology solutions for site visits, clinical monitoring, risk management and provide clinical operations colleagues with innovative ways to make a broader impact on the lives of the patients in our studies
- Oversee / manage projects to integrate and implement new technologies within clinical data capture or similar
- Manage the creation of new - and optimisation of existing - quality management processes
- Liaise with colleagues, eg within IT, Clinical Operations, Biometrics, QA & Regulatory Affairs, to ensure clinical trial activities are properly integrated / aligned to protocols
- Manage, implement, and develop solutions in site start-up, study recruitment/conduct, and data capture processes across multiple clinical technology programmes
- Act as a technical expert and leader within the business
- Drive best practice within the business
What you'll need to succeed
As well as strong communication skills for dealing with collaborators, stakeholders and vendors/CROs, you should have:
- A BSc (or equivalent experience) in a discipline such as computer science, biometrics, statistics, IT, or a life sciences discipline such as chemistry, biochemistry or biology
- Experience of the clinical drug development environment including experience in clinical software development and application deployment is essential, whether from a QA/CSV standpoint, or the data management/clinical operations side
- Deep expertise of regulatory requirements and industry standards relevant to clinical research, ensuring compliance throughout all stages of clinical trials
- Proven ability to design and/or develop technology solutions deployed in clinical trials – such as CTMS or other relevant technologies
Familiarity with navigating the clinical trial lifecycle and adhering to 21-CFR Part 11 regulations and validation processes
- Well-versed in the utilisation of common tools and technologies within clinical trials, including TMF, CTMS, DCT, and eSource, EDC, etc
- The ability to manage multiple concurrent projects and effectively prioritise between competing requirements
What you'll get in return
You'll get the chance to make a significant impact on the company's clinical development and R&D/discovery projects, taking on project leadership for a number of different aspects, driving the adoption of new protocols and processes to make their operations as innovative and effective as possible whilst maintaining compliance with regulatory standards.
The company are very flexible on salary bands and package depending on the skills of the person coming in and you will be a key member of a highly experienced team, with direct access to the C-suite leadership.What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on 0203 465 0057.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, especially as there are a number of other bioinformatics, data science and statistics positions available.
