Study coordinator Work, Jobs in Liverpool (with Salaries)

Study Coordinator
FutureMeds —Wirral
- Full-time
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- Data entry
Quick apply
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Mercury Hampton Ltd —Liverpool
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- Full-time
- CRM software
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Library and Academic Skills Coordinator
Coleg Cambria —Deeside
- £36,981 - £39,442 a year
- Full-time
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14d
Documentation Controller and Training Coordinator
Elanco —Speke
- Full-time
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Apprentice - Learning Support Administrator
Cheshire College South and West —Ellesmere Port
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5d
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Process Improvement Professional II
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Fuelius —Chester
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Study Coordinator

FutureMeds -
Wirral

Quick apply

Job details

Permanent | Full-time
23 hours ago

Benefits

Company pension
Private medical insurance

Qualifications

Management
Clinical research
Analysis skills
Data management
Data entry
Medical terminology
Communication skills

Full job description

FutureMeds: Shaping the Future of Clinical Research

Join us and become part of a team dedicated to excellence, collaboration, and the transformation of patient care through innovative research.

About FutureMeds

FutureMeds is a network of modern dedicated research sites conducting clinical trials. We find eligible patients for trials across a wide variety of therapy areas, helping pharmaceutical companies and contract research organisations to run clinical trials as efficiently and cost effectively as possible. Our priority is the safety and health of our patients and by helping to bring them future medicines today we can play a key part in improving health.

Position Overview

We are looking for a proactive and detail-oriented Study Coordinator to join the team at our busy Wirral site. In this key role, you will play an integral part in our clinical studies by maintaining meticulous documentation and strict adherence to protocols. You will ensure all records are kept to a high standard, keeping the site audit ready at all times.

The ideal candidate will bring prior experience as a Study Coordinator within a clinical research investigator site, with a comprehensive understanding of clinical trials and study protocols. Adept at meeting strict deadlines and possessing the flexibility to adapt and reprioritise tasks in a fast-paced environment. This is an exciting opportunity for an experienced Study Coordinator with a passion for clinical research, who is eager to take on a new role within an already thriving site. This role is based fully on-site at our Wirral clinic.

Key Responsibilities

Ensure accurate collection, entry and maintenance of clinical trial data
Monitor data consistency, completeness, and adherence to study protocols
Ensure all study deadlines are met
Collaborate with relevant teams to ensure quality and integrity of all study data
Always ensure strictest confidence and adherence to GDPR guidelines
Maintain records to ensure that the site remains audit ready at all times
Assist with preparation for internal and external audits and inspections, and contribute as required
Prepare data summaries and reports as required
Work closely with colleagues and sponsors to ensure seamless data flow
Support communication between teams to address data queries promptly
Ensure high-quality data is available at all times
Work closely and provide support to site clinical and administration teams
Communicate with clients by phone or email
Booking and rescheduling of monitor visits as required
Ensure prompt and accurate communication with sponsors and CRA’s
Communicate effectively and provide data as requested by the Site Director
Contribute to meetings with study sponsors/CROs, site clinical or full team meetings

Qualifications and Skills

Experience as a Study Coordinator within a clinical research environment is desirable.
Experience in a commercial healthcare setting preferable.
Strong attention to detail and accuracy in data entry and record-keeping.
Excellent communication skills, both written and verbal.
Ability to prioritise tasks and manage time effectively to meet deadlines.
Proactive problem-solving skills and a collaborative approach to working with cross-functional teams.

Benefits

Competitive salary package
Comprehensive benefits package including pension, life assurance, private healthcare and bonus
A dynamic working environment that celebrates success and rewards initiative
The chance to be part of making a meaningful contribution to the advancement of clinical research and healthcare

Job Types: Full-time, Permanent

Application question(s):

Will you now, or in the future, require visa sponsorship?

Experience:

Clinical Research: 2 years (preferred)
data entry/management: 2 years (required)

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

study coordinator jobs in liverpool

Study Coordinator

Business Development Coordinator

Library and Academic Skills Coordinator

Documentation Controller and Training Coordinator

Apprentice - Learning Support Administrator

CAD Systems and Facilities Coordinator

Process Improvement Professional II

Proposals Administrator

Senior Marketing Executive / Marketing Manager

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