Clinical trials associate Work, Jobs (with Salaries)

Clinical Research Associate II
Parexel —Remote
- Remote
- Bachelor's degree
- Computer skills
- Communication skills
Clinical Research Associate
BeiGene —Remote
- £42,900 - £53,600 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- English
12h
Clinical Research Associate - Midlands
MSD —London
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
Project Associate
ICON Plc —Swansea
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bachelor's degree
- Organisational skills
- Employee assistance programme
12h
Senior Research Associate, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Annual leave
Associate Scientist, Translational Medicine
Immunocore —Oxford
- Master's degree
- Bachelor's degree
- Organisational skills
8d
Clinical Trials Research Nurse
The Princess Alexandra Hospital NHS Trust —Harlow
- £39,959 - £48,117 a year
- Travel
13d
Clinical Support Associate
UHS Estates Ltd ( UEL ) —Southampton
- £39,959 - £48,117 a year
- Full-time
- Microsoft Excel
- Research
- Negotiation
- Annual leave
- Employee discount
5d
Senior Associate, Clinical Excellence
Reckitt —Kingston upon Hull
- Project management
- Employee assistance programme
- Life insurance
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
Parexel —Remote
- Remote
- Nursing
- Patient monitoring
- Bachelor's degree
Associate Consultant
Lumanity —London
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
1h
CEREBRIS Research Associate (Neurotechnology Trials Manager)
University of Bath —Bath
- £38,784 - £46,049 a year
- Full-time
- Doctoral degree
- University
- Presentation skills
- Annual leave
- Employee discount
1d
CRA
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
4d
(Associate) Medical Director - Neurology
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Communication skills
1d
Research Associate in ISAP study
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Research
7d
Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Doctoral degree
- Data analysis skills
- Annual leave

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Clinical Research Associate II

Parexel -
Remote

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Job details

Qualifications

Clinical research
Bachelor's degree
Computer skills
Communication skills

Full job description

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.

We are currently recruiting for Clinical Research Associate II to join our Multi-Sponsor Clinical Operations Team in the UK.

This role if fully decentralised in the UK.

Your time here

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.

As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you’ll do

Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you

On your first day we’ll expect you to have:

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Ability to perform all clinical monitoring activities independently.
Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
A client-focused approach to work and flexible attitude with respect to assignments/new learning.
The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
An honest and ethical work approach to promote the development of life changing treatments for patients.
Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

If you are ready to join Parexel’s Journey, please apply!

#LI-REMOTE

Apply Now

Refine Your Search

clinical trials associate jobs

Clinical Research Associate II

Clinical Research Associate

Clinical Research Associate - Midlands

Clinical Research Associate I

Associate (Clinical Outcome Assessments - COA)

Project Associate

Senior Research Associate, Bioanalytical & Molecular Assays

Associate Scientist, Translational Medicine

Clinical Trials Research Nurse

Clinical Support Associate

Senior Associate, Clinical Excellence

Drug Safety Associate II

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed

Associate Consultant

CEREBRIS Research Associate (Neurotechnology Trials Manager)

CRA

(Associate) Medical Director - Neurology

Research Associate in ISAP study

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

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