Careers at Glasgow Memory Clinic

Current Vacancies

Glasgow Memory Clinic Ltd specialises in research into the development of new treatments for memory impairment, Alzheimer's disease and dementia. We are a growing company which is on the forefront of clinical trials development. Our past success and our future is dependent on having the best people employed in roles that are exciting and interesting.

That is why we take recruitment of our people very seriously. We focus on not only the skills relevant to each role but also on other attributes that indicate the potential for long term mutually beneficial work relationships and career development. We offer stability, good quality of work, opportunities for progression and an impressive environment in which to work. We are an equal opportunities employer.

We currently have the following opportunities:

Medical Doctor

Developing new treatments for Alzheimer's - Glasgow Memory Clinic Ltd is an independent research clinic that works with healthy volunteers and patients in pioneering studies  of new treatments for Memory Impairment, Prodromal Alzheimer’s Disease, Alzheimer’s Disease and Dementia. Founded in 1999 we are considered to be one of the leading international centers in this area of clinical research.

Due to our continued growth, we seek additional doctors to join our expanding research team. Previous research experience is not required and a background in GP/Medicine/Geriatrics/Psychiatry/Neurology would be suitable. Clinical activities focus on screening and monitoring subjects involved in our trials. Full and part time positions are available. 

We offer great opportunities for a successful career in research and are developing a group of leading doctors who have a keen interest in research and an interest in helping us to develop and grow our successful clinic further. Our first class facility and working environment is based in  and West of Scotland Science Park, Bearsden. We offer an excellent remuneration package and family friendly working conditions. Further information about our Clinic can be found at

If you would like to join our enthusiastic and experienced team please send your CV without delay to

Apply for this job by downloading our application form on the right and emailing the filled out application to us at

Clinical Study Manager (Full Time)

The purpose of this exciting new position is to:

·  Develop, implement and deliver good management processes for smooth running of clinical trials

·  Contribute to a high performing clinic and strong team, providing expertise to generate top quality, accurate source documentation, manage EDC queries, assist with training requirements and help prepare site for audits and inspections.

·  Develop and maintain excellent  communication with sponsors, CROs ,CRAs and third party vendors

Minimum Requirements: 

·  A degree in scientific or health discipline or suitable medical or CRO working experience.

·  Demonstrable experience in clinical research with proven proficiency in trial execution.

·  Excellent site management capabilities with demonstrated capability to problem solve and mediate complex compliance issues.

·  Expert knowledge of international standards (GCP/ICH) and local regulations


Skill requirements;

·  Knowledge and experience of SDV and Site files.

·  Knowledge and experience of EDC and systems such as Inform and Rave.

·  Experience of previous audits and regulatory inspections would be advantageous.

·  Recognise potential challenges within the protocol and operational aspects of the trial and escalate to manager as appropriate/decide on appropriate action. 

·  Maintain a strong knowledge of the protocol to be able to answer standard operational questions from monitors, and local internal personnel. 

·  Ensure that study start-up activities and any amendments are conducted and completed on time.

·  Ensure documentation of training is up to date and provide training updates to staff as appropriate. 

·  Drive the conduct of the trials, track and oversee progress and status and ensure all operational aspects are on schedule. 

·  Communicate with field monitors on a regular basis to assure proper adherence to protocol, timelines and other trial related topics. 

·  Assist in facilitating internal audits and regulatory inspections as required. 

·  Prepare for and attend local investigator meetings as needed. 

·  Work with the Senior Manager (Quality) to ensure that all clinical trial related activities adhere to the requirements of current UK/EU legislation.

Apply for this job by downloading our application form on the right and emailing the filled out application to us at



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