Research Work, Jobs in Home Based (with Salaries)

Clinical Research Associate
BeiGene —Remote
- £42,900 - £53,600 a year
- Full-time
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- Microsoft Powerpoint
- Microsoft Word
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Research & Development Technician
MOUNTAIN PEAK TECHNOLOGY LTD —Remote
- £36,500 a year
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- Laboratory experience
- Bachelor's degree
Quick apply
8d
Research Analyst
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- £39,906 - £44,746 a year
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Clinical Research Associate II
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- Microsoft Word
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Senior Research Associate
IMD International Institute for Management Development —Remote
- £28,000.00 - £39,649.32 a year
- Full-time
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Market Research Telephone Interviewer
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Clinical Research Associate (CRA)
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Clinical Trial Associate (Associate, Rater Services)
Cogstate —Remote
- £50,000 - £55,000 a year
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Remote Software Developer – AI Research & Evaluation
Turing —Remote
- £200 - £300 an hour
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- Java
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- Annual leave
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21h
Application Scientist (India based)
Lhasa Limited —Remote
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10d
Equity Research Expert
Turing —Remote
- £100 - £200 an hour
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- English
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20h
Clinical Operations Manager (Data Review) - UK (homebased)
サイネオス・ヘルス —Remote
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Research Consultant - DACH (m/f/d)
Appinio —Remote
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Per Diem Research Nurse London UK
サイネオス・ヘルス —Remote
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New Business Manager Events Agency
MSL Global —Remote
- £50,000 - £55,000 a year
- Full-time
- Microsoft Powerpoint
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- Work from home
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Crypto Research Analyst
Crypto Banter —Remote
- Full-time
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- Research
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Global Business Marketing & Research Internship
Event Fusion Recruit —Remote
- From £12.80 an hour
- Remote
- Marketing
- Data analysis skills
- English
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10d
Philanthropy and Relationships Manager
Kids Charity —Remote
- £35,000 a year
- Full-time
- Travel
- Communication skills
5d
Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Writing skills
- English
Field Applications Scientist
Standard Biotools —Remote
- Full-time
- Doctoral degree
- Master's degree
- Travel

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Clinical Research Associate

BeiGene -
Remote

Apply Now

Job details

Full-time
£42,900 - £53,600 a year
7 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.

Apply Now

Refine Your Search

research jobs in home based

Clinical Research Associate

Research & Development Technician

Research Analyst

Clinical Research Associate II

Senior Research Associate

Market Research Telephone Interviewer

Clinical Research Associate (CRA)

Clinical Trial Associate (Associate, Rater Services)

Remote Software Developer – AI Research & Evaluation

Application Scientist (India based)

Equity Research Expert

Clinical Operations Manager (Data Review) - UK (homebased)

Research Consultant - DACH (m/f/d)

Per Diem Research Nurse London UK

New Business Manager Events Agency

Crypto Research Analyst

Global Business Marketing & Research Internship

Philanthropy and Relationships Manager

Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)

Field Applications Scientist

I want to receive the latest job alerts for research in home based

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