Associate Director

Top End jobs; Manchester; On-site; GBP 60,000 - 70,000; Full time

Job summary

A leading CRO in Manchester is seeking an Associate Director for their Small Molecule Bioanalysis function. The role entails providing high-level scientific leadership, managing a skilled team, and ensuring quality in bioanalytical outputs. Candidates should possess extensive experience in LC–MS/MS bioanalysis and have a strong track record in regulatory compliance. The compensation package includes a competitive salary of £60,000 - £70,000 and opportunities for career advancement.

Benefits

Competitive salary

Comprehensive benefits

Career advancement opportunities

Qualifications

• Extensive experience in LC–MS/MS bioanalysis within a CRO or life science organization.
• Proven record of leading LC-MS/MS method development and validation.
• Deep understanding of regulatory guidelines (FDA, EMA, ICH).

Responsibilities

• Lead and expand the small molecule bioanalysis capability.
• Oversee the design and validation of complex LC–MS/MS methods.
• Act as senior scientific lead for high-profile client programs.

Skills

LC–MS/MS bioanalysis experience

Scientific leadership

Regulatory guideline understanding

Project management

Collaborative leadership style

Education

PhD in Analytical Chemistry, Biochemistry or related discipline

Job description

ROLE: Associate Director
Location: Confidential
Contract Research Organization (CRO) supporting global pharmaceutical and biotechnology partners. As part of their continued expansion, they are seeking a senior scientific leader to head their Small Molecule Bioanalysis function. The associate scientific director will provide high-level scientific leadership, strategic direction, and technical oversight of a multi-levelled team of bioanalytical scientists. This position plays a pivotal role in shaping scientific strategy, driving innovation, and ensuring the highest quality of bioanalytical output across client studies.

About the Role

The associate scientific director will provide high-level scientific leadership, strategic direction, and technical oversight of a multi-levelled team of bioanalytical scientists.

Responsibilities

• Scientific Leadership & Strategy: Lead and expand the small molecule bioanalysis capability, setting scientific direction and ensuring alignment with regulatory expectations and industry best practice.
• Oversee the design, development, and validation of complex LC–MS/MS methods for quantitative bioanalysis in a range of biological matrices.
• Provide authoritative scientific guidance on study design, troubleshooting, assay strategy, and regulatory compliance (FDA, EMA, ICH).
• Drive scientific innovation, technology evaluation, and the implementation of new methodologies and instrumentation.
• Project Oversight & Client Engagement: Act as senior scientific lead for high-profile client programmes, ensuring successful delivery of complex bioanalytical studies.
• Build and maintain strong client relationships, articulating scientific rationales, presenting findings, and representing the bioanalytical team during audits and technical discussions.
• Contribute to the development of technical proposals, supporting business development with high-level scientific expertise.
• Team Leadership & Development: Provide mentorship, training, and leadership to scientists and principal investigators within the small molecule group.
• Ensure scientific integrity through detailed review and interpretation of complex data packages, reports, and validation summaries.
• Foster a culture of quality, collaboration, and continuous improvement within the laboratory.
• Operational & Departmental Responsibilities: Work closely with senior leadership to contribute to departmental growth, resource planning, and capability development. Champion process optimisation, workflow efficiency, and laboratory excellence across the bioanalytical function. Support cross-functional collaboration with quality, project management, and other scientific teams.

Qualifications

• Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline (PhD preferred; MSc considered with significant leadership experience).

Required Skills

• Extensive experience in LC–MS/MS bioanalysis within a CRO or life science organisation.
• Proven record of leading LC-MS/MS method development and validation programmes across discovery, nonclinical, and clinical stages.
• Deep understanding of regulatory guidelines (FDA, EMA, ICH) and their practical application to bioanalytical workflows.
• Strong track record of scientific leadership, including managing teams and overseeing complex project portfolios.
• Demonstrated ability to influence clients, defend scientific approaches, and lead high-level technical discussions.
• Experience in peptides, metabolites, or oligonucleotides is advantageous.
• Highly organised with strong decision-making ability and a collaborative leadership style.

Preferred Skills

• Experience in peptides, metabolites, or oligonucleotides is advantageous.

Pay range and compensation package

Competitive salary, comprehensive benefits, and exceptional opportunities for career advancement.

Equal Opportunity Statement

We are committed to diversity and inclusivity in our hiring practices.

Location: Manchester
Salary: £60,000 - £70,000 /annum
Relocation Package
Job Type: FullTime
Category: Medical/Pharmaceutical/Scientific