Clinical research Work, Jobs in Home Based (with Salaries)

Clinical Research Associate
BeiGene —Remote
- £42,900 - £53,600 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- English
6d
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 Trial Associate (Associate, Rater Services)
Cogstate —Remote
- £50,000 - £55,000 a year
- Remote
- Bilingual
- Computer literacy
- Bachelor's degree
Quick apply
Educational Advisor (Part time / Remote) - 12months project
SCRIBBLESENSE LTD —Remote
- Part-time
- Remote
- Research
- Bachelor's degree
- Recruiting
Quick apply
3d
Clinician to CRA - UK, FSP
Thermo Fisher Scientific —Remote
- Full-time
- Microsoft Word
- Writing skills
- English
3d
Clinical Data Programmer I
Clario —Remote
- Full-time
- Remote
- Computer Science
- Data analysis skills
- English
Medical Writer
Clario —Remote
- Full-time
- Remote
- Microsoft Word
- Doctoral degree
- Master's degree
- Annual leave
12d
Per Diem Research Nurse London UK
サイネオス・ヘルス —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Communication skills
Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
Parexel —Remote
- Remote
- Nursing
- Bachelor's degree
Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Writing skills
- English
Clinical Operations Manager (Data Review) - UK (homebased)
サイネオス・ヘルス —Remote
- Remote
- Nursing
- Bachelor's degree
- No degree
Principal Medical Writer - Publications
サイネオス・ヘルス —Remote
- Remote
- English
- Travel
- Mentoring
Clinical Team Manager, Respiratory, HIV & Hepatitis B
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Computer literacy
- Bachelor's degree
- Travel
13d
Project Manager II (EU or UK Based)
Clinical Ink —Remote
- Remote
- Business development
- Bachelor's degree
- No degree
Quick apply
FSP Principal Medical Writer (Regulatory) - Client-Dedicated
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Writing skills
- Project management
- Presentation skills
Single Sponsor Clinical Trial Manager / Local Study Manager - UK home based, within commuting distance of Reading
サイネオス・ヘルス —Remote
- Remote
- Bachelor's degree
- Team management
- Conflict management
(Associate) Medical Director - Neurology
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Communication skills
7d
Bank Mobile Research Nurse - Oxford/Reading/Basingstoke – Adult Nurse
WEP Clinical —Remote
- £1 an hour
- Remote
- Nursing
- Vital signs
- Medication administration
- Flexible schedule
Project Manager
Catalyst Clinical Research, LLC —Remote
- Full-time
- Remote
- Writing skills
- Analysis skills
- Bachelor's degree

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Clinical Research Associate

BeiGene -
Remote

Apply Now

Job details

Full-time
£42,900 - £53,600 a year
6 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

clinical research jobs in home based

Clinical Research Associate

Clinical Research Associate II

Clinical Research Associate (CRA)

Clinical Trial Associate (Associate, Rater Services)

Educational Advisor (Part time / Remote) - 12months project

Clinician to CRA - UK, FSP

Clinical Data Programmer I

Medical Writer

Per Diem Research Nurse London UK

Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed

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

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

Principal Medical Writer - Publications

Clinical Team Manager, Respiratory, HIV & Hepatitis B

Project Manager II (EU or UK Based)

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Single Sponsor Clinical Trial Manager / Local Study Manager - UK home based, within commuting distance of Reading

(Associate) Medical Director - Neurology

Bank Mobile Research Nurse - Oxford/Reading/Basingstoke – Adult Nurse

Project Manager

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

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