Clinical document 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
10d
Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance programme
Medical Coordinator
Public Sector Resourcing —Remote
- Full-time
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- IT
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Clinical Research Associate II
Parexel —Remote
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- Bachelor's degree
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Label Coordinator - Client dedicated
Thermo Fisher Scientific —Remote
- Full-time
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- English
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HR Advisor
Vita Health Group —Remote
- £30,000 - £32,000 a year
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Medication Management Specialist - Non-Medical Prescriber
Clinical Partners Ltd —Remote
- £60,000 a year
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Associate Clinical Operations Manager - FSP
Thermo Fisher Scientific —Remote
- Overtime
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Clinical Analyst -UK
GeneDx —Remote
- £89,000 - £108,000 a year
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Client Liaison Manager
HCML —Remote
- £28,000 - £32,500 a year
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Country Approval Specialist - FSP
Thermo Fisher Scientific —Remote
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The MDU —Remote
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Thermo Fisher Scientific —Remote
- Full-time
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- English
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Senior CTM - Neuroscience
Thermo Fisher Scientific —Remote
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CTM/Sr CTM - EMEA - FSP
Thermo Fisher Scientific —Remote
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Senior Medical Writer – Client Aligned (FSP)
Thermo Fisher Scientific —Remote
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Project Manager
Catalyst Clinical Research, LLC —Remote
- Full-time
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- Microsoft Office
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FSP Principal Medical Writer (Regulatory) - Client-Dedicated
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Project management
- Presentation skills
- Bachelor's degree
4d
Global Clinical Trial Leader - Sponsor Dedicated - Home based
Parexel —Remote
- Remote
- Management
- Master's degree
- Project management

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clinical document jobs near remote

Clinical Trial Assistant

Scout Clinical -
Remote

Quick apply

Job details

Full-time
£35,000 - £43,000 a year
10 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

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Refine Your Search

clinical document jobs in remote

Clinical Trial Assistant

Clinical Research Associate (CRA)

Medical Coordinator

Clinical Research Associate II

Label Coordinator - Client dedicated

HR Advisor

Medication Management Specialist - Non-Medical Prescriber

Associate Clinical Operations Manager - FSP

Clinical Analyst -UK

Client Liaison Manager

Country Approval Specialist - FSP

Dental Telephone Adviser

Principal Medical Writer (Publications)

Senior CTM - Neuroscience

Senior Regulatory Affairs Associate

CTM/Sr CTM - EMEA - FSP

Senior Medical Writer – Client Aligned (FSP)

Project Manager

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Global Clinical Trial Leader - Sponsor Dedicated - Home based

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