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Remote Pharmaceutical Research Jobs in Raleigh, NC

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Conduct remote monitoring activities appropriate for observational studies, including review of ...

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Remote Travel: Approximately 35% travel required, with overnight travel representing approximately ...

... pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

... pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

... pharmaceutical regulations and codes. This is a remote role but may require onsite visits to ... Demonstrated ability to critically analyze research design, methods, and outcome measures.

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Remote Pharmaceutical Research information

What is remote pharmaceutical research?

Remote pharmaceutical research refers to conducting various stages of drug discovery and development work from a location outside of a traditional laboratory or company office, often from home. This can include data analysis, literature reviews, clinical trial monitoring, regulatory documentation, and virtual collaboration with research teams. Advances in digital tools, secure data sharing, and teleconferencing have made it possible for many pharmaceutical research tasks to be performed remotely, increasing flexibility and access to a global talent pool.

How does collaboration typically work for professionals in remote pharmaceutical research roles?

In remote pharmaceutical research roles, collaboration is highly reliant on digital communication tools such as video conferencing, shared data platforms, and project management software. Researchers regularly participate in virtual meetings to discuss study progress, analyze data, and coordinate tasks with multidisciplinary teams, including scientists, regulatory specialists, and project managers. While working remotely can present challenges such as time zone differences and communication delays, most organizations have established structured workflows and regular check-ins to ensure alignment and maintain productivity. Strong written and verbal communication skills are essential for success in these roles.

What are the key skills and qualifications needed to thrive in remote pharmaceutical research, and why are they important?

To thrive in Remote Pharmaceutical Research, you need a solid background in life sciences or pharmacy, strong analytical skills, and experience with clinical research methodologies, often supported by an advanced degree. Familiarity with statistical analysis software, electronic data capture (EDC) systems, and regulatory compliance tools like Good Clinical Practice (GCP) certifications is crucial. Exceptional attention to detail, effective written communication, and self-motivation are valuable soft skills for remote collaboration and data interpretation. These skills ensure the integrity, accuracy, and regulatory compliance of research conducted outside traditional lab environments.

What are the most commonly searched types of Pharmaceutical Research jobs in Raleigh, NC?

The most popular types of Pharmaceutical Research jobs in Raleigh, NC are:

What are popular job titles related to Remote Pharmaceutical Research jobs in Raleigh, NC?

For Remote Pharmaceutical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Pharmaceutical Research jobs in Raleigh, NC look for?

The top searched job categories for Remote Pharmaceutical Research jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Pharmaceutical Research jobs?

Cities near Raleigh, NC with the most Remote Pharmaceutical Research job openings:

Infographic showing various Remote Pharmaceutical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Clinical Research Associate II / Senior Clinical Research Associate

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago


Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

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.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

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 request here.

Are you a current ICON Employee? Please click here to apply