Clinical research associate ii Work, Jobs (with Salaries)

Clinical Research Associate II
Parexel —Remote
- Remote
- Bachelor's degree
- Computer skills
- Communication skills
Clinical Research Associate II
IQVIA —Reading
- No degree
Clinical Research Associate II, South West England
IQVIA —Bath
- Maintenance
- No degree
Associate II, TMF Operations - UK - Remote
Worldwide Clinical Trials —England
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Administrative experience
Regulatory Associate - UK Medicines
Reckitt —Slough
- Data analysis skills
- Communication skills
- Employee assistance programme
- Life insurance
Project Manager II
Clinical Ink —Remote
- Remote
- Project management
- Bachelor's degree
- No degree
Quick apply
4d
Clinical Associate Professor in Spinal Surgery
Imperial College London —Hammersmith
- £113,565 - £150,569 a year
- Full-time
- Doctoral degree
- Rehabilitation centre
12h
Sr/CRA I/II - UK (numerous locations)
Thermo Fisher Scientific —Remote
- Full-time
- English
- Microsoft Office
- Presentation skills
Research Fellow in Brain Vascular Biology and Brain Cancer Biology
University College London —London
- £43,374 - £51,860 a year
- Full-time
- Doctoral degree
- English
- University
- Annual leave
- Employee assistance programme
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
3d
National Contact Point - Health (Cluster 1)
Innovate UK —Remote
- £58,589 a year
- Full-time
- Remote
- Presentation skills
- No degree
- In-person
6d
Senior Research Assistant (History and/or Philosophy of Science)
Manchester Metropolitan University —Manchester
- £33,002 a year
- Full-time
- Hybrid work
- Doctoral degree
- Communication skills
- Life insurance
Translational Medicine Expert – Dermatology, Associate Director
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Doctoral degree
- GP surgery experience
- English
Senior Respiratory Clinical Physiologist
Liverpool Heart & Chest Hospital NHS Foundation Trust —Liverpool
- Full-time
- Bachelor's degree
- IT
- Leadership
3d

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Clinical Research Associate II
Parexel —Remote
Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate…
Clinical Research Associate II
IQVIA —Reading
Requires at least 2 years on-site monitoring experience of interventional studies. Ensure copies/originals (as required) site documents are available for filing…

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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 research associate ii jobs

Clinical Research Associate II

Clinical Research Associate II

Clinical Research Associate II, South West England

Associate II, TMF Operations - UK - Remote

Regulatory Associate - UK Medicines

Project Manager II

Clinical Associate Professor in Spinal Surgery

Sr/CRA I/II - UK (numerous locations)

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

CRA

National Contact Point - Health (Cluster 1)

Senior Research Assistant (History and/or Philosophy of Science)

Translational Medicine Expert – Dermatology, Associate Director

Senior Respiratory Clinical Physiologist

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