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Clinical Research Rater Remote Jobs in Raleigh, NC

Clinical Project Lead, Oncology

Durham, NC ยท Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... clinical research. Key Responsibilities Clinical Trial Delivery & Oversight * Lead end-to-end ...

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 ...

... remote). This position will involve analyzing patient data and coordinating analysis of patient ... Manage, store, and analyze clinical research data Conduct systematic literature reviews, develop ...

Remote US or Canadian based. Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project ...

... the clinical research needs of global biopharmaceutical, biotechnology, medical device ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

... the clinical research needs of global biopharmaceutical, biotechnology, medical device ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

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Clinical Research Rater Remote information

See Raleigh, NC salary details

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How much do clinical research rater remote jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for clinical research rater remote in Raleigh, NC is $22.08, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $25.24 per hour, depending on experience, location, and employer.

What is a Clinical Research Rater (Remote)?

A Clinical Research Rater (Remote) is a professional who works from a remote location to assess and evaluate participants in clinical research studies. They are responsible for administering psychological or cognitive assessments, interviews, and questionnaires to study subjects according to research protocols. The data they collect is used to determine the effectiveness and safety of medical treatments or interventions being studied. This position requires strong attention to detail, excellent communication skills, and the ability to follow standardized procedures. Remote raters typically collaborate with research teams via secure digital platforms and may require specific certifications or training.

What are the key skills and qualifications needed to thrive as a Clinical Research Rater (Remote), and why are they important?

To thrive as a Clinical Research Rater (Remote), you need a background in psychology, neuroscience, or a related field, along with experience in clinical research and administering standardized assessments. Familiarity with electronic data capture (EDC) systems, clinical trial protocols, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, strong organizational skills, and the ability to communicate clearly with research teams are crucial soft skills. These abilities ensure accurate data collection, adherence to study protocols, and high-quality research outcomes in a remote environment.

What are some typical challenges faced by remote Clinical Research Raters, and how can they be addressed?

Remote Clinical Research Raters often face challenges such as maintaining consistent communication with study teams and ensuring accurate, unbiased assessments when working independently. To address these, it's important to establish clear protocols for virtual collaboration, regularly attend team meetings, and utilize secure data management systems. Staying organized and proactively reaching out for clarification when needed can help maintain high-quality data collection and foster a supportive remote work environment.

What is the difference between Clinical Research Rater Remote vs Clinical Data Entry Specialist?

AspectClinical Research Rater RemoteClinical Data Entry Specialist
Required credentialsHigh school diploma or equivalent; some roles may require clinical or research experienceHigh school diploma or equivalent; data entry skills preferred
Work environmentRemote, flexible hours, often part-timeRemote or on-site, regular hours, often full-time
Employer and industry usagePharmaceutical companies, research organizations, clinical trial sitesHealthcare providers, research organizations, hospitals

While both roles involve working remotely in the healthcare and research industry, Clinical Research Rater Remote focuses on evaluating patient data and clinical outcomes, whereas Clinical Data Entry Specialists primarily input and manage clinical data. The roles differ in responsibilities, with the former emphasizing assessment and analysis, and the latter concentrating on data accuracy and entry.

What are the most commonly searched types of Clinical Research Rater jobs in Raleigh, NC? The most popular types of Clinical Research Rater jobs in Raleigh, NC are:
What are popular job titles related to Clinical Research Rater Remote jobs in Raleigh, NC? For Clinical Research Rater Remote jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Clinical Research Rater Remote jobs? Cities near Raleigh, NC with the most Clinical Research Rater Remote job openings:

Director, Business Development

SiteBridge Research, Inc.

Raleigh, NC โ€ข On-site, Remote

Other

Posted 28 days ago


Job description

About SiteBridge:

Founded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The SiteBridge network extends reach further into these communities to empower a broader set of patients with some of the highest unmet needs to take part in clinical research to improve health outcomes.

Job Description: Director, Business Development

The Director, Business Development will help lead SiteBridge's commercial growth through key partnerships and expansion of SiteBridge research studies, inclusive of Sponsor, CROs and other channel partners. In this role, the Director will identify, prioritize, contact, and build relationships with Pharmaceutical/Biotech companies and CROs which the SBR site network can support with new clinical trial opportunities. This role works closely with internal departments including Feasibility, Study Start-Up, Operations, and Site Leadership to ensure timely communication and successful business development efforts. The ideal candidate is highly organized, professional, detail-oriented, and capable of managing multiple sponsor and CRO communications in a fast-paced clinical research environment.

The position will report to the Chief Executive Officer or Chief Operations Officer.

The position may be located in the Raleigh/Durham area though serious consideration will be given to remote candidates with the prerequisite experience.

Responsibilities:ย 

  • Develop and maintain professional relationships with Sponsors, CROs, pharmaceutical companies, and research partnersย 
  • Conduct outreach to Sponsors and CROs regarding upcoming and active clinical trial opportunities
  • Schedule introductory meetings, capability presentations, and feasibility discussionsย 
  • Serve as a point of contact for business development inquiries and follow-up communications
  • Identify new clinical trial opportunities aligned with the company's therapeutic areas, site capabilities and patient communitiesย ย 
  • Evaluate and engage new commercial partners based on evolution of site footprint, patient reach and emerging industry trendsย 
  • Monitor industry trends, Sponsor pipelines, and clinical trial databases for potential opportunities or partnerships
  • Collaborate with site leadership and investigators to evaluate interest and feasibility for studies
  • Support attendance and participation in industry conferences, networking events, and Sponsor meetingsย 
  • Assist with preparation of company presentations, capability decks, and marketing materialsย 
  • Represent the company professionally during external meetings and events
  • Gather site metrics including patient population, recruitment capabilities, previous trial experience, and enrollment projectionsย 
  • Support preparation for Pre-Selection Visits (PSVs), qualification visits, and Sponsor presentations
  • ย Develop and maintain client and contact profiles in SBR commercial trackers and CRM tools
  • Collaborate with any additional inside sales and commercial team partners to optimize selling opportunities
  • Utilize key Industry-related databases to leverage understanding of ongoing drug development for SBR Site Network growth (e.g. clintrials.gov., Sponsor-Investor presentations and meetings, Trial/SiteTrove, Informa, etc.)

Qualifications:

  • Bachelor's degree in business, health or equivalent preferred
  • 3-5+ years' clinical research, healthcare, pharmaceutical industry, preferably on the site side of the business
  • Minimum of 1-2 years of experience in clinical research, healthcare, sales, or business development preferred
  • Demonstrated understanding or experience in drug development and clinical operations and knowledge of clinical research processes, Sponsors, CROs, and study start-up activities and site operations preferredย 
  • Thorough knowledge of proposal development for business relationships
  • Thorough knowledge of clinical research and pharmaceutical industry, terminology and best practices
  • Strong and professional communicator and presenter, with ability to develop communications plans and follow-up cadence with key partners
  • Ability to manage multiple projects simultaneously and deliver in a deadline-driven environment
  • Demonstrated business acumen based on success in other roles which reflect critical thinking for strategic plans, business growth and expansion planning, contracts negotiations, etc.
  • Ability to work effectively in a fast-paced, innovative and high-growth environmentย ย 
  • Proficiency in Microsoft Office (Outlook, Excel, Word, and PowerPoint), CRM tools and business analytic tools
  • Demonstrated success in other roles which reflect collaborative and effective partnering with business and executive leaders, and an ability to influence decisions across functions
  • Ability to work independently and collaboratively in a cross functional team environment.ย 
  • Ability to travel as needed up to 50% time commitment at certain times
  • Occasional evening and weekend work may be required

SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements and individual qualifications and performance.