Office Based, Line Manager of Clinical Site Start-Up Group
Job Type :
Permanent
Job Location :
United Kingdom, South East, Berkshire
Job Salary :
£40000 - £50000 per annum + Full details on request
Job Description :
Perm: Berkshire Office Based, Line Manager of Clinical Site Start-Up Group – 50+ Associates
Contact Information: Lee Dunn Tel: +44 (0) 207 255 6665 Lee.dunn@1st-pharmapeople 1st-pharmapeople
Job Summary:
The purpose of this role is to Line Manage the Site Start-Up Group of over 50 associates that ensures fast patient recruitment and start-up for both local studies and complex multi-site, multinational studies. The role is Office based within one of the largest, most successful global CROs.
Offers:
This offers the chance to Line Manage one of the largest, fastest growing and most important teams with the Pharmaceutical/CRO industry. The role is run out of Berkshire offices for an industry leading and extremely successful CRO. The salary with this position ranges from 40,000.00 - 48,000.00 + benefits and relocation aid where appropriate.
Candidates:
Candidates for this role will need a Life Sciences Degree or equivalent. This combined with at least 6 years experience within Clinical research amongst CROs and Pharmaceutical companies. Candidates will need a minimum of 3 uninterrupted years experience in a leading/management capacity. Candidates will also need: Full knowledge of drug development process; Full knowledge of applicable regulatory requirements, SOPs, and company's Corporate Standards; Strong knowledge of budget management and resourcing; Considerable working knowledge of medical terminology; Ability to lead and motivate teams and the ability to handle management/personnel issues. A valid visa will need to be in place if needed and a valid UK or international driving is essential and non-negotiable.
Responsibility Brief:
A brief and short breakdown of responsibilities is here. A full and detailed breakdown can be supplied upon application: Interface with internal contacts to determine operational strategy and expectations and parameters for the review and negotiation of contracts and regulatory documents. Provide Proposal Management with input on proposals and budget development for SSU components of projects. Attend proposal defenses as needed. Create Investigator Grant Estimates for Proposal Management, as necessary. Work with sponsors and internal team members to establish regulatory requirements and contracts necessary for SSU components of projects. Review and negotiate regulatory documents, contracts, and contract amendments with sponsors for agreement on wording and budgets. Ensure accuracy and completeness of documents. Where applicable, review and ensure project work instructions for SSU projects are completed and accurate. Provide feedback to SSU leads in the writing of project work instructions. Interact with Clinical Operations, Project Ma
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