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Remote Merck Clinical Trials Jobs in Raleigh, NC

micro1 AI

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

micro1 AI

Director of Biostatistics

Durham, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

micro1 AI

Biostatistician

Durham, NC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

... clinical trials, and ensure the highest standards of patient care, data quality, and regulatory ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

M3USA

Participant Recruitment Analyst

Raleigh, NC · Remote

... clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness ... This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ...

M3USA

Participant Recruitment Analyst

Raleigh, NC · On-site +1

... clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness ... This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ...

IQVIA

Freelance Independent Rater

Raleigh, NC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Durham, NC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Raleigh, NC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Durham, NC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

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All JobsMerck Clinical Trials JobsRemote Merck Clinical Trials JobsRemote Merck Clinical Trials Jobs in Raleigh, NC

Remote Merck Clinical Trials information

See Raleigh, NC salary details

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$79

How much do remote merck clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote merck clinical trials in Raleigh, NC is $41.88, according to ZipRecruiter salary data. Most workers in this role earn between $35.53 and $41.83 per hour, depending on experience, location, and employer.

What is a remote Merck clinical trial?

Remote Merck Clinical Trials are research studies conducted by Merck & Co., Inc. that allow participants to take part from their homes or other locations outside of traditional clinical sites. These trials use digital technologies, such as telemedicine, mobile apps, and wearable devices, to monitor participants, collect data, and communicate with study teams. Remote trials aim to make participation more convenient, increase patient diversity, and improve data collection. They may include virtual visits, home delivery of study medications, and remote monitoring of health outcomes. This approach helps expand access to clinical research while maintaining the safety and integrity of the study.

How do remote team members in Merck clinical trials collaborate with on-site staff and ensure seamless trial operations?

Remote team members in Merck Clinical Trials utilize secure digital platforms for communication, data management, and document sharing to stay connected with on-site colleagues. Regular virtual meetings, clear scheduling, and standardized protocols help bridge the distance and maintain alignment on clinical trial milestones. Collaboration tools such as electronic trial master files (eTMF) and project management software are commonly used to track progress and address challenges promptly. This structure enables remote staff to contribute effectively to trial operations, support patient recruitment, and monitor compliance while maintaining efficiency and strong team integration.

What are the key skills and qualifications needed to thrive as a remote clinical trials specialist at Merck?

To excel as a Remote Clinical Trials Specialist at Merck, you generally need a background in life sciences or healthcare, experience in clinical research, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and sometimes certifications like SOCRA or ACRP are commonly required. Strong organizational skills, attention to detail, and effective remote communication are essential soft skills for managing study protocols and collaborating with diverse teams. These competencies are crucial for ensuring regulatory compliance, data integrity, and the efficient coordination of clinical research activities from a remote setting.

What is the difference between Remote Merck Clinical Trials vs Remote Clinical Research Associate?

AspectRemote Merck Clinical TrialsRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonSame as Merck Clinical Trials, often requiring similar degrees and certifications
Work EnvironmentRemote, often within pharmaceutical or biotech companies like MerckRemote, working on clinical trial sites or for research organizations
Employer & Industry UsagePrimarily employed by pharmaceutical companies like Merck, focusing on clinical trial managementEmployed by CROs or pharmaceutical companies, focusing on site monitoring and trial coordination

Both roles involve clinical trial work with similar credentials and work environments. The main difference is that Remote Merck Clinical Trials refers to roles within Merck's clinical trial programs, while Remote Clinical Research Associates typically work across various organizations, focusing on site monitoring and trial coordination.

What are the most commonly searched types of Merck Clinical Trials jobs in Raleigh, NC?

The most popular types of Merck Clinical Trials jobs in Raleigh, NC are:

What are popular job titles related to Remote Merck Clinical Trials jobs in Raleigh, NC?

For Remote Merck Clinical Trials jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Merck Clinical Trials jobs in Raleigh, NC look for?

The top searched job categories for Remote Merck Clinical Trials jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Merck Clinical Trials jobs?

Cities near Raleigh, NC with the most Remote Merck Clinical Trials job openings:

Remote Merck Clinical Trials jobs near you
Infographic showing various Remote Merck Clinical Trials job openings in Raleigh, NC as of August 2026, with employment types broken down into 78% Full Time, 9% Part Time, and 13% Contract. Highlights an 100% Remote job distribution, with an average salary of $87,117 per year, or $41.9 per hour.

Biostatistician

micro1 AI

Raleigh, NC • Remote

$60 - $65/hr

Part-time

Posted 20 days ago

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks that require deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
  2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
  3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
  4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
  5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
  6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.


Preferred Qualifications

  1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
  2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
  3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
  4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
  5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
  6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
  7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.

Apply