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From Home Cra Monitor Jobs in Raleigh, NC (NOW HIRING)

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project ... Supporting the management team with training, process improvements, co-monitoring visits, mentoring ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project ... Supporting the management team with training, process improvements, co-monitoring visits ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

From clinical trials to regulatory, consulting, and market access, every clinical development ... Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

From clinical trials to regulatory, consulting, and market access, every clinical development ... Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported ...

MiCo2 Group LLC

Pledge Drive 1.1

Smithfield, NC · On-site

$24K - $32K/yr

Dual monitors recommended Benefits WhyYou'll Love It: * Start at $13-$15/hour * Set your own hours * Growth and promotion opportunities * Work from the comfort of home If you are dedicated ...

MiCo2 Group LLC

Pledge Drive 1.1

Smithfield, NC · On-site

$13 - $15/hr

Dual monitors recommended Benefits WhyYou'll Love It: * Start at $13-$15/hour * Set your own hours * Growth and promotion opportunities * Work from the comfort of home If you are dedicated ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project ... Supporting the management team with training, process improvements, co-monitoring visits,mentoring ...

Community Based Care

In-home aide

Wake Forest, NC · On-site

$12.50 - $16/hr

Monitoring vitals and patient behavior and reporting them to the nursing and medical staff ... Assisting patients with mobility needs, transferring them from wheelchair to bed * Turning or ...

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$10.7K

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How much do from home cra monitor jobs pay per year?

As of Aug 21, 2026, the average yearly pay for from home cra monitor in Raleigh, NC is $77,219.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,100.00 and $132,700.00 per year, depending on experience, location, and employer.

What is a from home CRA monitor?

Work From Home CRA (Clinical Research Associate) Monitors are professionals who oversee clinical trials and research studies remotely. They ensure that clinical sites comply with protocols, regulatory requirements, and good clinical practice guidelines. By working from home, CRAs use digital tools to monitor data, communicate with site staff, and manage documentation, reducing the need for frequent on-site visits. This role requires strong organizational, communication, and technical skills to maintain the integrity of clinical research while working remotely.

What skills and qualifications are needed to thrive as a from home CRA monitor?

To thrive as a Home-based CRA Monitor, you need a solid background in life sciences or a related field, previous clinical research experience, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and regulatory documentation is typically required, along with relevant certifications such as ACRP or SOCRA. Strong organizational skills, attention to detail, self-motivation, and effective communication are crucial soft skills for managing remote responsibilities and collaborating with study sites. These skills ensure the quality and compliance of clinical trials while enabling efficient remote oversight and accurate reporting.

What are common challenges faced by a from home CRA monitor and how can they be managed?

As a Work From Home CRA (Clinical Research Associate) Monitor, one of the main challenges is maintaining effective communication with on-site staff and ensuring data integrity remotely. Without being physically present, it can be harder to build rapport and quickly resolve site issues. Utilizing robust virtual meeting tools, scheduling regular check-ins, and ensuring thorough documentation can help overcome these challenges. Adapting to new technologies and being proactive in communication are key to success in this remote role.

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Clinical Trial Lead

Allucent

Cary, NC • On-site, Remote

Full-time

Re-posted 7 days ago

Job description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial activities on a global, multi-country, or regional basis. The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
Responsibilities
As an expert in Clinical Trial Leadership, you are:
  • Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline, budget, quality, productivity) are met.
  • Liaising closely with the Project Manager (PM) and other department leaders if /when necessary, on all trial-related issues and service delivery.
  • Supporting the management team with training, process improvements, co-monitoring visits, mentoring of staff and / or any other special assignments within Global Clinical Operations.

Requirements
To be successful you will possess:
  • A degree in life sciences or nursing qualification preferred, but not required.
  • A minimum of 5 years of clinical research experience with at least 2-years' CTL or other relevant experience.
  • In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical trials
  • Strong therapeutic background in oncology
  • Possesses experience and knowledge in the CRO industry that will support Allucent's management of clinical trials
  • Strong written and verbal communication skills including professional command of English language to communicate with internal and external stakeholders on a daily basis.

Benefits
Benefits of working at Allucent include:
  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program

Disclaimers:
*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.
"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."
#LI-Remote #LI-Hybrid #LI-TCW

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