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- Tasks: Lead bioanalytical studies, ensuring compliance and quality throughout the process.
- Company: ACM Global Laboratories is a specialist analytical facility focused on bioanalytical services.
- Benefits: Enjoy a sign-on bonus, flexible working hours, and opportunities for professional growth.
- Why this job: Join a dynamic team dedicated to quality and innovation in the bioanalytical field.
- Qualifications: B.Sc in Chemistry and 6+ years of study management experience required.
- Other info: Position based in York, UK with a Monday to Friday schedule.
The predicted salary is between 48000 - 72000 £ per year.
ACM Global Laboratories – Sr. Study Manager Small Molecule
Job Title: Sr. Study Manager Small Molecule
Category: Other
Closing Date: 22/10/2025
Department: BioA
Location: York, UK
Schedule: Days; Monday – Friday
Sign On Bonus: Up to 25% Sign-On/Relocation Bonus Available
SUMMARY
ACM Bioanalytical Services (BioA) is a specialist analytical facility that provides a service measuring low concentration analytes (e.g. sub nanogram per milliliter) in biological matrices. The post-holder is expected to work efficiently and effectively to supply sponsors with an efficient and effective service.
RESPONSIBILITIES
- Act as Study Manager/Principal Investigator for regulatory and non-regulatory studies.
- Ensure studies are conducted in compliance with company SOPs, policies, protocols, study plans, analytical methods, and regulatory standards.
- Responsible for generating Study Plans, Data Transfer Agreements, Analytical Reports, and subsequent amendments.
- Document and complete any quality documentation (Quality issue, CAPA, deviation, change control) as appropriate and within the required timeframes.
- Responsible for addressing all study-related internal audit comments.
- Act as departmental lead with Sponsor/Client/internal teams for Bioanalytical activities conducted on assigned studies.
- Participate in internal and external quality assessment activities as required.
- Oversee LC-MS/MS method development and troubleshooting.
- Provide technical, practical, and scientific direction for work conducted.
- Ensure all data is archived in accordance with company SOPs and regulatory requirements.
- Review any protocol, study plan, report, SOP, or scientific paper as required.
- Be knowledgeable of current concepts and principles of GLP, GCP, and COSHH and how to conduct work and supervise others to ensure compliance.
- Follow the company’s Standard Operating Procedures (SOPs) and maintain an individual training file.
- Take the lead in procedural updates and training required in response to changes/updates to regulatory and industry standards affecting the department.
- Communicate effectively with team members and discuss ideas in an open and professional manner.
- Manage schedules and commitments effectively, considering personnel, periods of leave, facilities, and equipment.
- Promote best practices within working areas.
- Drive the ACM Mission, Vision, and Core Values with every interaction.
- Foster a culture that promotes quality, safety, ethical practices, customer focus, and service.
- Support the effective performance of the team and individuals to ensure operational schedules align with ACM commitments and client expectations.
- Monitor study-specific budgets and operational costs, contributing to proposal amendments as needed.
- Ensure management is informed in a timely and transparent manner about daily operations and any deviations from goals or objectives.
- Own operational improvements and implement measures for enhanced compliance, productivity, and profitability.
- Understand ACM\’s business and work scope in relation to study costs and the impact of changes.
- Support new business development activities, including providing information for new sales inquiries (RFIs, RFPs).
- Collaborate with Commercial and Management teams to drive new business and expand the Bioanalytical Services offering.
- Recognize issues and potential issues, making informed decisions on resolution/prevention.
- Understand personal knowledge limitations and escalate issues where necessary.
- Lead teams through change processes, addressing obstacles and maintaining engagement.
- Drive process improvements and develop/training junior team members.
- Collaborate and integrate with the wider ACM organization.
REQUIRED QUALIFICATIONS
- B.Sc in Chemistry or related subject.
- Minimum of 6 years study management experience in regulated bioanalysis.
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ACM Global Laboratories - Sr. Study Manager Small Molecule employer: Glasgows
Contact Detail:
Glasgows Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land ACM Global Laboratories - Sr. Study Manager Small Molecule
✨Tip Number 1
Familiarise yourself with the latest GLP and GCP guidelines, as well as ACM's specific SOPs. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality in bioanalytical services.
✨Tip Number 2
Network with professionals in the bioanalytical field, especially those who have experience with small molecule studies. Attend relevant conferences or webinars to make connections and gain insights that could be beneficial during your application process.
✨Tip Number 3
Prepare to discuss your experience with LC-MS/MS method development and troubleshooting in detail. Be ready to share specific examples of challenges you've faced and how you resolved them, as this is a key responsibility for the role.
✨Tip Number 4
Showcase your leadership skills by preparing examples of how you've successfully managed teams through change processes. Highlighting your ability to foster a positive team culture and drive operational improvements will set you apart from other candidates.
We think you need these skills to ace ACM Global Laboratories - Sr. Study Manager Small Molecule
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Sr. Study Manager position at ACM Global Laboratories. Tailor your application to highlight relevant experience in study management and bioanalysis.
Craft a Strong CV: Your CV should clearly outline your educational background, particularly your B.Sc in Chemistry or related subjects, and detail your 6+ years of study management experience. Use bullet points to emphasise key achievements and responsibilities that align with the job description.
Write a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Highlight specific experiences that demonstrate your ability to manage studies in compliance with regulatory standards and your familiarity with GLP, GCP, and COSHH principles.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for the role of Sr. Study Manager.
How to prepare for a job interview at Glasgows
✨Understand the Role Thoroughly
Before the interview, make sure you have a solid grasp of the responsibilities and requirements of the Sr. Study Manager position. Familiarise yourself with ACM Global Laboratories' services, especially in bioanalytical studies, to demonstrate your knowledge and enthusiasm.
✨Prepare for Technical Questions
Given the technical nature of the role, be ready to discuss your experience with LC-MS/MS method development and troubleshooting. Brush up on GLP, GCP, and COSHH principles, as well as any relevant analytical methods, to showcase your expertise.
✨Showcase Your Leadership Skills
As a Study Manager, you'll need to lead teams and manage projects effectively. Prepare examples from your past experiences where you've successfully led a team or managed a project, highlighting your ability to drive process improvements and foster a collaborative environment.
✨Demonstrate Effective Communication
Effective communication is key in this role. Be prepared to discuss how you've communicated with clients, sponsors, and internal teams in the past. Highlight your ability to convey complex information clearly and professionally, as well as how you handle feedback and discussions.
