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Job description

Job Brief:

Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyse clinical data.

Job Responsibilities:

• Design and implement clinic strategies in compliance with the business goals.
• Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
• Develop advertising and other informational materials to be used in subject recruitment.
• Oversee subject enrolment to ensure that required documents are properly obtained and archived.
• Inform patients or caregivers about study aspects and outcomes to be expected.
• Monitor study activities to ensure compliance with protocols and with all relevant regulators and institutional policies.
• Coordinate with ethics committees to safeguard the rights, safety, and well-being of all research subjects and research activities
• Instruct research staff in scientific and procedural aspects of studies.
• Order drugs or devices necessary for study completion.
• Contact outside healthcare providers and communicate with subjects to obtain follow-up information.

Job Requirements:

• Minimum four years experience in clinical data work, nursing, academic or pharmaceutical research, clinical coordinators, or clinical trials administrators.
• A Bachelor's degree in nursing, pharmacy, or other health-related fields.
• Strong written and oral communication skills
• Strong interpersonal skills
• Leadership skills and ability to provide technical guidance, advice and support to professional staff where needed
• Superior problem-solving, deductive reasoning and decision-making skills
• Good time management and ability to prioritise tasks and accomplish set goals efficiently
• Knowledge of statistical data collection, validation, editing, and analysis techniques
• Knowledge of laboratory certification processes and standards
• Excellent attention to detail and ability to maintain detailed and accurate records
• You should be comfortable completing administrative tasks in an efficient and productive manner.

Why join AHRO? Experience the delight of:

• A welcoming and amiable ambience
• Being a part of a diverse team
• Empowering your creative spirit with authority

Job Types: Full-time, Permanent

Salary: £32,000.00-£38,000.00 per year

Benefits:

• Casual dress
• Flexitime
• Sick pay

Schedule:

• Flexitime
• Holidays
• Monday to Friday

Ability to commute/relocate:

• Glasgow: reliably commute or plan to relocate before starting work (required)

Work authorisation:

• United Kingdom (required)

Work Location: In person