Programme Lead - Clinical Delivery
Posted 3 hours ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Program Lead in Clinical Delivery, to join a company in the pharmaceutical industry, at their site based in Bracknell, on a contract basis for 12 months.
Salary:
Hourly rate of between £39.00 - £52.00 PAYE (inside IR35).
Program lead, Clinical Delivery role:
Your Background:
Company:
Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.
Location:
This role is based at our clients site in Bracknell. You will be working 3 days in the office, and 2 days remotely.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 108 203 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Salary:
Hourly rate of between £39.00 - £52.00 PAYE (inside IR35).
Program lead, Clinical Delivery role:
- Lead the creation and execution of the exploratory and biopharmaceutics clinical development plans at a molecule level.
- Technical leadership and operational oversight of clinical research trials within the development plan.
- Responsible for planning and delivering exploratory and biopharmaceutics clinical molecules and submissions milestones on time and on budget throughout the molecule lifecycle.
- Responsible for all aspects of global clinical trial operations within the plan.
- You will be the single operational point of contact from trial design through execution and close out, including timeline creation and management, outsourcing plan, vendor management (including direct oversight of the operational deliverables), patient recruitment and retention and budget management.
Your Background:
- Bachelor’s degree in a science related field from an accredited college or university.
- 3-years’ + experience in the pharmaceutical industry with direct experience of managing clinical studies, ideally in exploratory and biopharmaceutics clinical development (5+ year preferred).
- Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials.
- Ability to influence and oversee TPOs to enable delivery of trial level deliverables.
- Demonstrated knowledge and experience with project management tools and processes.
- Demonstrated ability to work effectively cross-culturally and in a virtual work environment.
- Demonstrated ability to influence both internal and external environments appropriately and forge strong working relationships.
Company:
Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.
Location:
This role is based at our clients site in Bracknell. You will be working 3 days in the office, and 2 days remotely.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 108 203 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
- Type:
- Contract
- Start Date:
- ASAP
- Contract Length:
- 12 months
- Contact Name:
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- Telephone:
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- Job Reference:
- V-108203
- Job ID:
- 222622250
- Applications:
- Less than 10
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