Skip to main content
Post your CV and find your next job on Indeed!

clinical trial assistant jobs

Sort by: -
    • Knowledge of compliance management related to clinical trials and research regulations.
    • Proven supervising experience within clinical or research settings.
    • Experience with venepuncture and basic clinical observations.
    • Maintain confidentiality and data protection standards (GDPR, trial-specific SOPs).
    • The post holder is a recognised expert in Ophthalmology and in the field of clinical research, providing advice, care and support to patients entering clinical…
    • View all London North West University Healthcare NHS Trust jobs - London jobs
    • Salary Search: Research Project Manager salaries in London
    • See popular questions & answers about London North West University Healthcare NHS Trust
    • This role will provide excellent experience of randomised controlled trials, working with NHS services and would suit individuals interested in going on to…
    • The Clinical Research Fellow will be required to undertake a leading role in the initiation and delivery of clinical research studies and clinical trials ,…
    • Take formal minutes in meetings (for example in trial steering group committees for national trials with more than 15 members of all levels of experience) and…
    • The roles are ideal for individuals who are keen to develop their experience in clinical trials administration.
    • Ensuring all clinical trials are conducted according to Protocol, recruiting patients who are eligible for the study.
    • Annual Leave Buy and Sell Scheme.
    • The Greater Manchester Clinical Research Delivery Centre (GM CRDC) is a collaborative infrastructure supporting the rapid delivery of early-phase and commercial…
  • View similar jobs with this employer
    • Knowledge of medical terminology, and an interest in clinical trials/drug development – desirable.
    • Medpace is a full-service clinical contract research…
  • View similar jobs with this employer
    • This position plays a key role in the clinical trial management process at Medpace.
    • Medpace is a full-service clinical contract research organization (CRO)…
    • Experience in research, innovation, knowledge exchange, or partnership development, particularly in any of the health, well-being and clinical sciences…
  • View similar jobs with this employer
    • Assisting with the preparation of tax computations for individuals and companies.
    • Assisting more senior colleagues in gathering information and communicating…
  • View similar jobs with this employer
    • Our Tax teams are responsible for managing and handling various aspects of taxation for individuals, businesses, and organisations.
    • Attend training sessions on specialist software required for specific research trial data capture.
    • Liaising with the study leads and clinical staff to assist…

People also searched:

regulatory affairs entry level
clinical trial coordinator
clinical trials
pharmacovigilance
clinical trial assistant entry level
officer
pa
personal assistant
secretary
support

Job Post Details

Clinical Research Site Manager - job post

Medica Research
Yorkshire
£45,000 - £55,000 a year - Full-time

Job details

Pay

  • £45,000 - £55,000 a year

Job type

  • Full-time

Location

Yorkshire

Benefits

Pulled from the full job description

  • Referral programme
  • Employee discount
  • Company pension
  • Company events

Full job description

Overview

We are seeking a dynamic and detail-oriented Clinical Research Site Manager to lead and oversee the operations of our clinical research sites. This pivotal role involves managing day-to-day activities, ensuring compliance with regulatory standards, and fostering a collaborative environment that drives research forward. The ideal candidate will bring a proactive leadership style, experience in clinical research, and a passion for advancing health through meticulous project management. Join us to play a vital role in pioneering innovative research initiatives that make a real difference.

Duties

  • Lead the planning, coordination, and execution of clinical research studies at the site, ensuring adherence to protocols and regulatory requirements
  • Supervise and mentor research staff, fostering a team-oriented environment focused on excellence and continuous improvement
  • Oversee participant recruitment, enrollment, and retention processes to meet study timelines and objectives
  • Maintain rigorous compliance with Good Clinical Practice (GCP), Study Protocols, and other regulatory standards
  • Manage site targets, resources, and inventory to optimize operational efficiency
  • Ensure accurate documentation and data integrity throughout all stages of research activities
  • Collaborate with vendors, internal and external teams to facilitate smooth study progress and resolve issues promptly

Requirements

  • Proven supervising experience within clinical or research settings
  • Strong background in scientific or clinical research methodologies and protocols
  • Demonstrated project management skills with the ability to coordinate multiple tasks simultaneously
  • Laboratory experience or familiarity with laboratory procedures is highly desirable
  • Knowledge of compliance management related to clinical trials and research regulations
  • Leadership qualities that inspire teamwork, accountability, and high performance
  • Excellent communication skills for effective collaboration with diverse stakeholders

Join us as a Research Site Manager to lead innovative projects that push the boundaries of science! Your expertise will directly contribute to groundbreaking discoveries while supporting a collaborative environment committed to excellence. We value your dedication to advancing health through meticulous research management.

Pay: £45,000.00-£55,000.00 per year

Benefits:

  • Company events
  • Company pension
  • Employee discount
  • Referral programme

Work Location: In person

Let Employers Find YouUpload Your Resume