Job Description
SUMMARY
The Clinical Trial Scientific Affairs Analyst is responsible for the review of study protocols and investigating testing requirements to assist in facilitating the timely response for proposals. Coordinates the testing methods as needed with ACM Research and Development, ACM Laboratory, and referral laboratory partners for study support and set up. Obtains and document testing information throughout the course of the active trial.
OFFERINGS
- Auto Enrolment Pension
- Comprehensive Benefits Package
- Working within a Global organisation
- Career Advancement Opportunities including Apprenticeships
STATUS: Full Time
LOCATION: Remote Based – UK
DEPARTMENT: Scientific Affairs
SCHEDULE: Days;Monday—Friday
At ACM Global Laboratories our employees are empowered to progress in a career that creates purposeful and meaningful work. ACM impacts the medical field with over 500 Clinical Trials and 2 million CT tests annually.
AWARDS & RECOGNITION
- Top 10 Most Trusted Clinical Laboratory in 2021
ATTRIBUTES
- BSc required in life science
- 3- 5 yrs experience as a Clinical Laboratory Scientist in a medical diagnostic laboratory or central laboratory
- Excellent communication, word processing, and computer skills
- Excellent interpersonal and communication skills
- Excellent time management and organizational skills
- Ability to manage multiple projects with tight deadlines
- Be familiar and comply with Good Clinical Practice (GCP) and / or Good Laboratory Practice (GLP) appropriate to the work performed.
RESPONSIBILITIES
- Scientific Analysis. Investigate testing requirements and testing facilities to identify required testing and associated nuances through the course of the study. Provide scientific/technical information to compile client RFIs. Provide data support to the Medical Director to address analytical trends or issues. Provide consultation to clinical trials operations and external clients as needed. Coordinate the testing methods as needed with referral labs. Obtain and document referred testing information throughout the course of the active trial.
- Collaboration. Maintain referral laboratory relationships. Liaises with sales staff to participate in client teleconferences to address new business needs or ongoing study issues. Assumes responsibility for channeling information to and from Laboratory Operations and Sales.
- Quality & Regulatory. Investigate and implement corrective actions as needed. Investigate issues during the life cycle of studies. Investigate issues with referral laboratories. Works with Supervisor/Manager to update global SOPs as needed. Makes suggestions to manager for improved work methods and ways to increase efficiency, reduce costs, and solve operational problems. Understands and follows company policies and procedures and respecting patient confidentiality.
Job Type: Full-time
Benefits:
- Company pension
- Employee discount
- Health & wellbeing programme
- Referral programme
- Work from home
Schedule:
- Day shift
- Monday to Friday
- No weekends
Application question(s):
- Will you now or in the future require sponsorship?
Education:
Experience:
- Laboratory Sample Analysis: 3 years (required)
Work Location: Remote
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