Clinical trial monitor Work, Jobs in Scotland (with Salaries)

Clinical Research Coordinator
Dr Xantia Clinical Research Services —Aberdeen
- £36,000 - £42,000 a year
- Full-time
- Microsoft Word
- English
- Data entry
Quick apply
2d
Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Livingston
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
11d
Executive Director of Clinical Business Development - Strategic Accounts
サイネオス・ヘルス —Glasgow
- Remote
- Google Suite
- Salesforce
- Microsoft Office
Executive Director of Clinical Business Development - Strategic Accounts
Syneos Health Commercial Solutions —Glasgow
- Remote
- Google Suite
- Salesforce
- Microsoft Office
Supervisor, Specimen Management
IQVIA —Livingston
- Full-time
- Bachelor's degree
- Continuous improvement
- Team management
Manager, Process Excellence
Catalent —Bathgate
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
- Free parking
- Employee assistance programme
13d
Management Accountant
Piramal Pharma Solutions Inc. —Grangemouth
- Data analysis skills
- Analysis skills

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Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Livingston
Implement data transfer mechanisms for external data streams (into CDR) including access for external data providers. Experience working on clinical trials.
11d
Management Accountant
IDOX plc —Glasgow
Part-qualified, finalist or fully qualified accountant (ACCA, CIMA, ICAS or equivalent). Also, please note successful applicants will need to satisfy the BPSS…
£28,265.24 - £53,506.96 a year
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3d

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clinical trial monitor jobs near scotland

Clinical Research Coordinator

Dr Xantia Clinical Research Services
Aberdeen

Quick apply

Job details

Permanent | Full-time
£36,000 - £42,000 a year
2 days ago

Qualifications

Microsoft Word
Healthcare research operations
Clinical research
Patient appointment coordination
English
Data entry
Project schedule tracking
Good Clinical Practice (GCP)
English
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination
Project progress tracking
Progress tracking

Full job description

About the Role

This role is suitable for an organised healthcare or life-sciences professional who can coordinate clinical research activities, maintain accurate study documentation, and support researchers throughout the delivery of clinical studies.

You will work closely with investigators, research nurses, clinicians, study participants, laboratories, sponsors, and administrative teams to ensure that research projects are conducted efficiently, ethically, and in accordance with approved study protocols.

Key Responsibilities

Coordinate day-to-day activities across assigned clinical research studies.
Schedule participant visits, assessments, follow-up appointments, and study procedures.
Maintain accurate study files and essential research documentation.
Support participant screening and recruitment activities.
Review study eligibility requirements and flag potential participants for clinical review.
Prepare study documentation for investigator and research-team use.
Track participant enrolment, retention, and study completion.
Maintain screening logs, enrolment logs, and study trackers.
Coordinate laboratory tests, sample collections, and specimen-processing requirements.
Ensure research data is entered accurately into study databases.
Review study records for missing or inconsistent information.
Support investigators with regulatory and ethics documentation.
Assist with amendments, approvals, and study-document updates.
Prepare documentation for monitoring visits, audits, and inspections.
Coordinate communication with research sponsors and external study partners.
Track adverse-event documentation and escalate clinical concerns appropriately.
Monitor study timelines and outstanding research activities.
Maintain investigational-product or study-material records where applicable.
Support participant communications and approved appointment reminders.
Prepare regular study-progress and recruitment reports.

What We Are Looking For

At least 2–3 years of experience in clinical research, healthcare administration, life sciences, research support, or a related role.
Experience maintaining clinical or research documentation.
Strong organisational and record-management skills.
Excellent attention to detail and data accuracy.
Ability to coordinate several studies or research activities simultaneously.
Understanding of patient confidentiality and healthcare data protection.
Strong communication skills when working with clinicians, participants, and research partners.
Ability to follow detailed study protocols and operating procedures.
Good working knowledge of Microsoft Word, Excel, Outlook, and digital record systems.
Ability to manage deadlines and follow up on outstanding documentation.
Strong written and spoken English.
A degree or professional qualification in life sciences, healthcare, biomedical science, psychology, nursing, or a related discipline is preferred.

Preferred Skills

Experience working within clinical trials or healthcare research.
Knowledge of Good Clinical Practice principles.
Experience using electronic data-capture systems.
Familiarity with clinical-trial management systems.
Experience supporting ethics or regulatory submissions.
Knowledge of informed-consent and participant-recruitment procedures.
Familiarity with research governance requirements.
Experience supporting monitoring visits or research audits.
Understanding of adverse-event reporting processes.
Experience working with pharmaceutical, biotechnology, university, or hospital research teams.
Current Good Clinical Practice training is desirable.

Mindset

You are precise, dependable, and comfortable working in an environment where documentation quality is essential. You understand that clinical research depends on following approved protocols, maintaining accurate records, and protecting the rights and confidentiality of study participants.

You communicate clearly, raise discrepancies early, and take responsibility for completing study activities on schedule. You recognise the boundaries of a coordination role and refer clinical decisions or participant-safety concerns to appropriately qualified research

Pay: £36,000.00-£42,000.00 per year

Work Location: In person

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clinical trial monitor jobs in scotland

Clinical Research Coordinator

Data Acquisition Specialist - External Data (Remote - UK)

Executive Director of Clinical Business Development - Strategic Accounts

Executive Director of Clinical Business Development - Strategic Accounts

Supervisor, Specimen Management

Manager, Process Excellence

Management Accountant

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