Clinical study Work, Jobs in Remote (with Salaries)

Clinical Trial Assistant
Scout Clinical —Remote
- £35,000 - £43,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick apply
14d
Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance programme
Clinical Research Associate II
Parexel —Remote
- Remote
- Bachelor's degree
- Computer skills
- Communication skills
Clinical Research Associate
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
12d
Label Coordinator - Client dedicated
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Customer service
- English
- Microsoft Office
6d
Clinical Case Manager
Lyra Health —Remote
- £30,000 - £35,000 a year
- Part-time
- Remote
- Computer literacy
- Bachelor's degree
- Typing
- Employee assistance programme
Senior Clinical Research Associate I
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
12d
Clinical Data Programmer I
Clario —Remote
- Full-time
- Remote
- Computer Science
- English
- Microsoft Office
Country Approval Specialist - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Organisational skills
Single Sponsor Clinical Trial Manager / Local Study Manager - UK home based, within commuting distance of Reading
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- Bachelor's degree
- Contracts
- Computer skills
2d
Senior Clinical Research Associate II
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
12d
Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Project Manager II
Clinical Ink —Remote
- Remote
- Project management
- Bachelor's degree
- No degree
Quick apply
12d
Contract Specialist - FSP
Thermo Fisher Scientific —Remote
- 8 hour shift
- Remote
- English
- Organisational skills
- Contracts
Senior Regulatory Affairs Associate
Simbec-Orion —Remote
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
Regional Clinical Compliance Manager
BeiGene —Remote
- £63,200 - £79,000 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Outlook
- English
5d
Senior CTM - Neuroscience
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Microsoft Outlook
- English
- Bachelor's degree
4d
Regulatory Affairs Manager - Regulatory Liaison - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Microsoft Office
- Master's degree
21h
Associate Director, Regulatory Affairs - UK & Ireland
BeiGene —Remote
- £80,700 - £100,900 a year
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Office
- Bachelor's degree
Strategic Proposal Writer
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel

I want to receive the latest job alerts for clinical study in remote

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical study jobs near remote

Clinical Trial Assistant

Scout Clinical -
Remote

Quick apply

Job details

Full-time
£35,000 - £43,000 a year
14 days ago

Qualifications

Microsoft Excel
Microsoft Outlook
Clinical research
Customer service
Microsoft Office
Bachelor's degree
Computer skills

Full job description

Established in 1996 and rebranded to Scout in 2024, we built our foundation on planning meetings for numerous organizations within the life sciences sector (Scout Meetings). In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient reimbursements and travel.

Scout is recognized as a leader in our field for innovation in service, attention to detail, our stellar team members, and making the complex easier. If this interests you, we’d love to have you join our rapidly growing team!

Position Summary:

The Clinical Trial Assistant plays an integral role in the successful execution of Scout studies, collaborating closely with Project Management teams to ensure operational excellence and high-quality delivery across all trial activities.

Responsibilities of this position include but are not limited to:

Oversee and coordinate assigned study activities in partnership with Project Managers, ensuring all operational milestones are achieved throughout the study lifecycle
Maintain and monitor study calendars, scheduling onboarding, training sessions, and key project meetings to support seamless study execution
Manage the preparation, review, and finalization of study documentation and required reports
Communicate proactively with external stakeholders, including client operations teams, to facilitate efficient document flow
Configure and manage study setups within the Scout Clinical portal, including user credentials and access management
Collaborate cross-functionally with internal teams, such as the Patient Liaison group
Manage client-facing communications, including shared mailboxes, ensuring timely and professional responses
Process and track invoices for translation and other study-related services, as needed
Send customer surveys and compile survey data
Manage virtual card payments, ScoutPass distribution
Minor technical support for Scout portal users
Contribute to organizational initiatives, supporting leadership with special projects and operational enhancements as needed
Complete all required initial and ongoing training within the required timeframe

The ideal candidate will have the following experience, skills, and knowledge:

BS or BA degree or equivalent experience preferred
1-2 years of experience with clinical research is a strong plus
Strong computer skills (Excel, Word, Outlook, Internet Explorer)
Knowledge and understanding of foreign currency and ability to convert to USD

The ideal candidate will have the following competencies and qualities:

Ability to work independently, handle multiple projects/tasks simultaneously
Ability to track and manage key dates/deadlines
Timely, professional, courteous correspondence and communication with clients, vendors, and colleagues
Eager to learn and develop, with a high level of coachability and a growth mindset
Excellent Interpersonal skills
Attention to Detail
Extremely Customer Service Oriented
Patient, Flexible Attitude
Thrive in fast-paced environments, maintaining performance under pressure
Self-motivated and results-driven, while following instructions to achieve optimal outcomes
Good Communicator / Articulate
Proficient with MS Office Suite, especially Excel

Visit our website at www.scoutclinical.com or follow us on LinkedIn for other employment opportunities.

WE ARE AN EQUAL OPPORTUNITY EMPLOYER

DjLjBhUuAf

Quick apply

Refine Your Search

clinical study jobs in remote

Clinical Trial Assistant

Clinical Research Associate (CRA)

Clinical Research Associate II

Clinical Research Associate

Label Coordinator - Client dedicated

Clinical Case Manager

Senior Clinical Research Associate I

Clinical Data Programmer I

Country Approval Specialist - FSP

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

Senior Clinical Research Associate II

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

Project Manager II

Contract Specialist - FSP

Senior Regulatory Affairs Associate

Regional Clinical Compliance Manager

Senior CTM - Neuroscience

Regulatory Affairs Manager - Regulatory Liaison - FSP

Associate Director, Regulatory Affairs - UK & Ireland

Strategic Proposal Writer

I want to receive the latest job alerts for clinical study in remote

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected