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- Tasks: Investigate testing requirements and support clinical trials operations with data analysis.
- Company: Join a leading health organisation focused on innovative clinical research.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by optimising clinical trial processes.
- Qualifications: Bachelor’s degree and experience in Biomedical Science or clinical trials.
- Other info: Collaborative environment with a focus on process improvement and career advancement.
The predicted salary is between 36000 - 60000 £ per year.
The Clinical Trial Scientific Affairs (CTSA) Post-Award Analyst is responsible for investigating testing requirements and testing facilities to assist in facilitating the timely response for internal study operations team. The CTSM Post Award Analyst has proficient knowledge in laboratory science and assists with process improvement initiatives within Scientific Affairs.
RESPONSIBILITIES- Ensures complete study scoping, including testing requirements, facilities and other nuances.
- Provides technical details to ACM study team for study designs and updates.
- Provides data support to address analytical trends or issues.
- Provides consultation to clinical trials operations and external clients, as needed.
- Responsible for channeling information to and from Laboratory Operations and Study Management.
- Conducts investigations and assists with implementation of corrective actions, as needed.
- Investigates issues during the life cycle of the studies.
- Manages low to medium complex assignments.
- Assists with special projects, as needed.
- Participates in cross functional process improvement initiatives to optimize operational capabilities.
- Serves as a laboratory science expert for study optimization.
- Participates in quality issue investigations, documentation and resolutions.
- Understands and follows company policies and procedures, respecting patient confidentiality.
- Performs other duties as assigned.
- Bachelor’s Degree.
- Minimum 1 year Biomedical Science experience AND clinical trials experience OR 2 years Biomedical Science experience.
- Clinical Trials experience.
- Strong communication and interpersonal skills.
- Ability to multitask, working on multiple projects with tight deadlines.
- Strong Microsoft Office skills.
- Generalist laboratory background.
S - Sedentary Work - Exerting up to 10 pounds of force occasionally. Sedentary work involves sitting most of the time, but may involve walking or standing for brief periods of time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
For disease specific care programs refer to the program specific requirements of the department for further specifications on experience and educational expectations, including continuing education requirements.
Any physical requirements reported by a prospective employee and/or employee’s physician or delegate will be considered for accommodations.
Clinical Trials Scientific Affairs Analyst employer: ACM Global Laboratories, Inc.
Contact Detail:
ACM Global Laboratories, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Scientific Affairs Analyst
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical trials field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. We want you to show off your knowledge about their work in clinical trials, so dive deep into their website and any recent publications.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to your experience in biomedical science and clinical trials. We suggest doing mock interviews with friends or using online resources to boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Clinical Trials Scientific Affairs Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trials Scientific Affairs Analyst role. Highlight your relevant experience in biomedical science and clinical trials, and don’t forget to showcase your strong communication skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your background makes you a perfect fit for our team. Keep it concise but impactful!
Showcase Your Technical Skills: Since this role involves providing technical details and data support, be sure to mention your proficiency with Microsoft Office and any other relevant tools. We love seeing candidates who can multitask and manage complex assignments!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team!
How to prepare for a job interview at ACM Global Laboratories, Inc.
✨Know Your Science
Brush up on your laboratory science knowledge and be ready to discuss how it applies to clinical trials. Be prepared to explain testing requirements and facilities, as this role heavily relies on your scientific expertise.
✨Showcase Your Communication Skills
Since the role involves liaising with various teams, practice articulating complex information clearly. Think of examples where you've successfully communicated technical details to non-technical stakeholders.
✨Demonstrate Problem-Solving Abilities
Prepare to discuss past experiences where you identified issues during study cycles and implemented corrective actions. Highlight your analytical skills and how they contributed to process improvements.
✨Familiarise Yourself with Company Policies
Understand the importance of patient confidentiality and company procedures. Be ready to discuss how you would ensure compliance in your role, showing that you respect both ethical standards and operational guidelines.