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Bachelor's degree in a relevant scientific discipline or healthcare-related field * Extensive ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Bachelor's degree in a relevant scientific discipline or healthcare-related field * Extensive ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
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Bachelor's degree in a relevant scientific discipline or healthcare-related field * Extensive ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
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... fully Remote position Key Responsibilities: * Serve as the organization's scientific expert ... Develop clinical protocols, study endpoints, biomarker strategies, and data collection ...
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Remote Clinical Scientist information
See Raleigh, NC salary details
$27.57 - $32.29
6% of jobs
$32.29 - $37
13% of jobs
$39.09 is the 25th percentile. Wages below this are outliers.
$37 - $41.72
14% of jobs
$41.72 - $46.43
11% of jobs
The median wage is $49.84 / hr.
$46.43 - $51.15
9% of jobs
$51.15 - $55.87
18% of jobs
$55.87 - $60.58
2% of jobs
$62.35 is the 75th percentile. Wages above this are outliers.
$60.58 - $65.30
6% of jobs
$65.30 - $70.01
3% of jobs
$70.01 - $74.73
7% of jobs
$74.73 - $79.44
11% of jobs
$27
$53
$79
How much do remote clinical scientist jobs pay per hour?
What is a remote clinical scientist?
A Remote Clinical Scientist conducts clinical research, analyzes data, and supports drug or therapy development while working remotely. They collaborate with cross-functional teams, including medical, regulatory, and biostatistics professionals, to ensure study integrity and compliance. Responsibilities may include protocol development, clinical trial monitoring, and scientific data interpretation. This role typically requires expertise in clinical research, regulatory guidelines, and therapeutic areas relevant to the employer’s focus. It allows professionals to contribute to clinical advancements without being tied to a physical location.
How does a remote clinical scientist collaborate with onsite teams and manage project responsibilities from a distance?
Remote Clinical Scientists work closely with clinical research associates, data managers, and investigators through frequent virtual meetings, collaborative platforms, and electronic documentation tools. They are responsible for reviewing data, monitoring trial progress, ensuring protocol compliance, and addressing site queries, all while maintaining regular communication with onsite staff. This remote setup requires proactive scheduling, timely reporting, and strong organizational skills to stay aligned with project milestones. The ability to leverage digital communication tools ensures effective teamwork and consistent project oversight despite physical distance.
What are the key skills and qualifications needed to thrive in the remote clinical scientist position, and why are they important?
To excel as a Remote Clinical Scientist, you typically need an advanced degree in a life science field, experience in clinical research, and strong data analysis skills. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and regulatory requirements such as GCP is crucial, as are relevant certifications like SOCRA or ACRP. Excellent communication, self-motivation, and problem-solving abilities set apart top candidates in this remote role. These skills ensure the effective oversight of clinical trials, compliance with regulations, and successful remote collaboration with multidisciplinary teams.
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Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 14 days ago
Job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
What You Will Do:
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Willingness to travel as required (approximately 60%)
#LI-LB1 #LI-REMOTE
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply