Job Details
My client is a fast-growing Contract Research Organisation (CRO) located near Macclesfield. They provide specialist bioanalytical services to support discovery and regulatory drug development programs. They provide services to support clients with small & large molecule, peptide, oligonucleotide and biomarker projects. Due to the ongoing growth, they are looking to add to the Project Leader Group. The ideal candidate is hardworking, ambitious and enthusiastic in building a career in scientific project management.
Responsibilities
- Be the key contact for clients for assigned projects
- Act as study director/ principal investigator/Project Leader for assigned studies
- Understand client requirements and timescales, liaising with business development executives in the production of quotes as required
- Maintain effective relationships with clients
- Review documentation for protocols and lab manuals
- Preparations of bioanalytical study or other plans
- Work as part of a team
- Review and sign of study data
- Responsible for regulatory compliance as assigned
- Ensure all processes are following GCP/GLP
- Liaising with clients within agreed timescales
Qualifications
- At least 3 years experience working in a regulatory bioanalytical laboratory.
- A degree in life sciences or a chemistry-related subject
- A good communicator with strong interpersonal skills.
- Experience of working within a GLP/GCP accredited facility.
- Flexible and adaptable with an eye to detail
- Hands-on experience of LC-MS/MS, Sciex and Waters LC-MS/MS systems is an advantage
- Experience in Bioanalytical method Development is an advantage
Benefits
- Competitive Salary
- Pension Scheme
- Flexible Working Hours
- Generous Holiday Package
- Career Progression Opportunities