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Contract Start-up Specialist
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A Contract Start-up Specialist job position has opened up at an international contract research organisation providing drug discovery, lifecycle management and laboratory services. With offices in over 45 countries and approximately 13,000 professionals, this company provide innovative ideas behind multiple sectors. This particular position will be based in Glasgow on permanent contract.
In this role you will draft, review and negotiate agreements with clinical study sites and principal investigators ("Clinical Trial Agreements"). Serve as the primary contact for all Clinical Trial Agreements for all clinical studies assigned to his/her group and must be able to work independently, while consulting with Company attorneys and other key individuals as appropriate and necessary. Draft and review CTA and associated contracts related to CTAs according to Company policy, rules, practices and procedures and implement and manage the process for internal and external approval, execution and filing of CTAs and associated contracts. Identify and assist with the implementation of process improvement opportunities. Maintain contact and relationships with all internal departments, Senior Management and clients and shall identify and protect PPD and its clients from unnecessary business and legal risk.
This is an office-based position and can be based in either our Cambridge, Glasgow or Winchester office.
Skills and Requirements:
- University degree will be an advantage
- Experience in contract drafting and negotiation experience
- Or equivalent combination of education and experience that provides the knowledge, skills, and abilities to perform the job
- Excellent communication and interpersonal skills
- Excellent organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively
- Preferable experience with the UK model clinical trials agreement
- Flexible and able to reprioritize workload to meet changing project needs
- Excellent MS Excel and MS Word skills
- Excellent English and grammar skills
- Excellent analytical and decision-based thinking
- Capable, with appropriate oversight, of drafting and negotiating contract provisions
- Must be able to work independently and as a team player
- Must be able to provide direction to other employees
- Responsible for understanding and adhering to the company and Client SOPs, WPDs and other regulations for all aspects of project implementation, execution and closeout.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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