Clinical research Work, Jobs (with Salaries)

Clinical Research Associate
BeiGene —Remote
- £42,900 - £53,600 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- English
4d
Clinical Research Associate II
Parexel —Remote
- Remote
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Organisational skills
- Communication skills
- Time management
- Employee assistance programme
Clinical Research Assistant
Riverstone Healthcare —Sutton
- £27,420.00 - £45,064.54 a year
- Full-time
- Patient monitoring
- Data analysis skills
- Analysis skills
Quick apply
Clinical Research Associate
Novo Nordisk —Gatwick Airport
- Travel
- Communication skills
- Time management
1d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
Clinical Research Trials Assistant
University of Oxford —Oxford
- £32,108 - £37,338 a year
- Full-time
- Microsoft Word
- Doctoral degree
- University
- Annual leave
Clinical Trial Associate (Associate, Rater Services)
Cogstate —Remote
- £50,000 - £55,000 a year
- Remote
- Bilingual
- Computer literacy
- Bachelor's degree
Quick apply
Clinical Research Nurse
Thermo Fisher Scientific —Glasgow
- Full-time
- Hospital
- Computer literacy
- English
Clinical Research Associate
IQVIA —Nottingham
- Full-time
- No degree
- Travel
- Recruiting
Clinical Research Fellow
University College London —London
- £52,748 - £81,260 a year
- Full-time
- Doctoral degree
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
1d
Clinical Research Coordinator/Cognitive Rater
Imperial College Healthcare NHS Trust —London
- £47,951 - £56,863 a year
- Full-time
2d
Clinical Research Associate - Midlands
MSD —London
- Full-time
- Writing skills
- Bachelor's degree
- Travel
Clinical Trials Coordinator
University College London —London
- £43,981 a year
- Full-time
- Hybrid work
9d
Clinical Research Practitioner
Kent Community Health NHS Foundation Trust —Wye
- £39,959 - £48,117 a year
- Part-time
- Patient care
9d
Clinical Trials Coordinator part time 0.5 FTE
University College London —London
- £21,990.50 a year
- Part-time
- Hybrid work
9d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
8d
Clinical Research Coordinator -Wolverhampton, UK
IQVIA —Wolverhampton
- Part-time
- Microsoft Word
- Bachelor's degree
- Data entry
Principal Scientist, Clinical Research - Remote UK
Leica Biosystems —Newcastle upon Tyne
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Bachelor's degree
Clinical Research Coordinator
Dr Xantia Clinical Research Services —Aberdeen
- £36,000 - £42,000 a year
- Full-time
- Microsoft Word
- English
- Data entry
Quick apply
1d

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Clinical Research Associate

BeiGene -
Remote

Apply Now

Job details

Full-time
£42,900 - £53,600 a year
4 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Clinical research
Stakeholder collaboration
English
Microsoft Office Suite
Clinical compliance monitoring
Organisational skills
Good Clinical Practice (GCP)
Microsoft Project
Communication skills
Good Clinical Practice (ICH-GCP) guidelines

Full job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.
May be assigned to CRA activities or start-up activities, depending on experience and project needs
Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region.
Identify gaps and areas for improvement and propose CAPA.
Supports start-up and provides local expertise.
The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.

CRA activities

Perform feasibility, site identification, selection and evaluation, preparing/supporting initial list of sites and recruitment targets
Provides protocol and related study training to assigned sites.
Conducts monitoring (pre-study, initiation, routine monitoring and closeout) visit per monitoring plan and applicable SOPs
Conducts co-monitoring visits, if required
Completes monitoring visit reports in accordance with ICH-GCP, BeOne standards and SOP
Manages sites and site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations
Ensure inspection readiness of the study and sites
Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.)
Attends disease indication project specific training and general CRA training as required
Facilitate Study Oversight Visits (SOVs), site audits and/or inspections, as required
Evaluates the quality and integrity of site practices – escalating quality and/or GCP issues with Investigators and internal team as appropriate.
Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating excellence, question status-quo and promote innovation.

Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook Other

Qualifications:

Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
Ideally 2-5 years of (CRA) monitoring experience in the pharmaceutical or CRO industry • Excellent communication and interpersonal skills
Excellent organizational skills and ability to prioritize and multi-task
Fluent in English (writing and speaking)

Travel: up to 60%

Salary Range 42,900.00 GBP - 53,600.00 GBP

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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Clinical Research Associate

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