Everest Clinical Research Jobs Hiring Now
Everest Clinical Research is hiring for 7 open roles on Migrate Mate as of July 16, 2026, concentrated in project management and data science, with listed salaries up to about $200,000. Migrate Mate updates Everest Clinical Research's live openings daily. Everest Clinical Research is a contract research organization providing biostatistics, data management, and clinical trial services to pharmaceutical and biotechnology clients.
Find Everest Clinical Research JobsOverview
Everest Clinical Research hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 7
- Top team
- Project Management
- Seniority
- Manager level or above
- Work type
- 100% remote or hybrid
- Top location
- Bridgewater
- Salary range
- $90,000–$200,000
Listed salaries for Everest Clinical Research roles on Migrate Mate range from about $90,000 to $200,000 per year across 7 open roles, as of July 16, 2026.
Open Roles at Everest Clinical Research
Showing 7 of 7+ Everest Clinical Research jobs
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Biostatisticians for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients. Provide day to day technical and operational leadership to project teams supporting these programs/projects.
Provide statistical oversight on projects in the assigned drug development programs/projects, ensuring sound statistical methodologies in study design, sample size estimation, statistical analysis planning, statistical modeling, data handling, analysis, and reporting.
Coach, mentor, develop, and provide technical review, advice and expertise to less experienced Biostatisticians as well as Statistical Programmers assigned to the program/projects.
Provide statistical input in protocol design and development. Participate in the writing of trial protocols and research proposals.
Serve as a primary biostatistician, working effectively with interdisciplinary teams to contribute strategically (through innovative ideas or applications) to drug development and commercialization at the study and drug compound/therapeutic areas levels.
Review and provide input to clinical data management deliverables, including but are not limited to the following: eCRFs, eCRF Completion Instructions, data validation specifications, Data Review Plan (and the ongoing data review tables, listings, and figures in accordance with the Plan), and Data Management Plan.
Write Statistical Analysis Plans, Statistical Reports, and statistical methodologies sections of Clinical Study Reports. Perform peer review of SAPs and other technical documents written by others.
Perform hands on statistical analysis and modeling, and maintains expertise in state-of-the-art statistical methodology and regulatory requirements.
Validate core statistical tables, listings, and figures programmed by statistical programmers and/or biostatisticians, ensuring that core results for each responsible trial are complete and accurate. Perform overall Quality Control review on statistical deliverables before they are released to the clients.
Review and confirm ADaM dataset specifications. Perform quality control activities on ADaM datasets programmed by other statistical programmers and biostatisticians.
Provide statistical consultation to medical and clinical trial personnel for the publication of trial results, and participate in the writing of abstracts, manuscripts, posters, and presentations.
Ensure all study level as well as drug program level statistical and programming activities are conducted in compliance with relevant regulatory requirements and applicable standards/conventions.
Interact with regulatory agencies and support sponsor in new drug application. This includes participating as a statistical liaison to the regulatory agency on behalf of the sponsor company and ensuring documentation, statistical results, and study datasets meet the regulatory agency’s requirement/expectation (e.g., CDISC).
Perform statistical and programming resource management, capacity analysis, benchmarking and metrics. Participate in the continuous improvement and maintenance of statistical and programming governing documents.
Contribute to organization development and growth by participating in the interview and evaluation process for professional applicants.
Qualifications and Experience:
A Ph.D. degree in statistical science, mathematical analysis or related fields with at least 7 years of relevant experience or a Master’s degree in these fields with at least 10 years of relevant experience, with demonstrated exceptional ability and performance.
Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $150,000 - $200,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com (http://www.ecrscorp.com).
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#LI-Remote
#LI-TK1
#INDHP
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Biostatisticians for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients. Provide day to day technical and operational leadership to project teams supporting these programs/projects.
Provide statistical oversight on projects in the assigned drug development programs/projects, ensuring sound statistical methodologies in study design, sample size estimation, statistical analysis planning, statistical modeling, data handling, analysis, and reporting.
Coach, mentor, develop, and provide technical review, advice and expertise to less experienced Biostatisticians as well as Statistical Programmers assigned to the program/projects.
Provide statistical input in protocol design and development. Participate in the writing of trial protocols and research proposals.
Serve as a primary biostatistician, working effectively with interdisciplinary teams to contribute strategically (through innovative ideas or applications) to drug development and commercialization at the study and drug compound/therapeutic areas levels.
Review and provide input to clinical data management deliverables, including but are not limited to the following: eCRFs, eCRF Completion Instructions, data validation specifications, Data Review Plan (and the ongoing data review tables, listings, and figures in accordance with the Plan), and Data Management Plan.
Write Statistical Analysis Plans, Statistical Reports, and statistical methodologies sections of Clinical Study Reports. Perform peer review of SAPs and other technical documents written by others.
Perform hands on statistical analysis and modeling, and maintains expertise in state-of-the-art statistical methodology and regulatory requirements.
Validate core statistical tables, listings, and figures programmed by statistical programmers and/or biostatisticians, ensuring that core results for each responsible trial are complete and accurate. Perform overall Quality Control review on statistical deliverables before they are released to the clients.
Review and confirm ADaM dataset specifications. Perform quality control activities on ADaM datasets programmed by other statistical programmers and biostatisticians.
Provide statistical consultation to medical and clinical trial personnel for the publication of trial results, and participate in the writing of abstracts, manuscripts, posters, and presentations.
Ensure all study level as well as drug program level statistical and programming activities are conducted in compliance with relevant regulatory requirements and applicable standards/conventions.
Interact with regulatory agencies and support sponsor in new drug application. This includes participating as a statistical liaison to the regulatory agency on behalf of the sponsor company and ensuring documentation, statistical results, and study datasets meet the regulatory agency’s requirement/expectation (e.g., CDISC).
Perform statistical and programming resource management, capacity analysis, benchmarking and metrics. Participate in the continuous improvement and maintenance of statistical and programming governing documents.
Contribute to organization development and growth by participating in the interview and evaluation process for professional applicants.
Qualifications and Experience:
A Ph.D. degree in statistical science, mathematical analysis or related fields with at least 7 years of relevant experience or a Master’s degree in these fields with at least 10 years of relevant experience, with demonstrated exceptional ability and performance.
Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $150,000 - $200,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com (http://www.ecrscorp.com).
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#LI-Remote
#LI-TK1
#INDHP
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
Job Roles at Everest Clinical Research
Working at Everest Clinical Research
Everest Clinical Research's 7 open roles are manager level or above, and about 100% are remote or hybrid. The most active teams are project management, data science, and biotech & life sciences. Everest Clinical Research is a contract research organization that supports clinical drug development by providing biostatistics, statistical programming, and clinical data management services to life sciences companies. Most Everest Clinical Research roles are based in Bridgewater.
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Browse jobs by roleEverest Clinical Research Jobs: Frequently Asked Questions
How many jobs is Everest Clinical Research hiring for right now?
Everest Clinical Research is hiring for 7 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in project management and data science. Roles span biostatistics, statistical programming, and clinical data management, with positions ranging from senior to principal level. Migrate Mate pulls the latest openings directly so the count reflects what is currently active.
What kinds of roles does Everest Clinical Research hire for?
The most active teams are project management, data science, and biotech & life sciences. Everest Clinical Research predominantly hires for clinical research professionals, including biostatisticians, statistical programmers, clinical data managers, and clinical database designers. Most postings are manager level or above, with titles at the senior and principal level common across all functional areas. Both remote and office-based positions appear regularly in the active openings.
Are Everest Clinical Research jobs remote or in-person?
Mostly remote. About 100% of Everest Clinical Research's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Bridgewater. Each Everest Clinical Research listing shows its work location so you can filter before applying.
How do I apply to a job at Everest Clinical Research?
Find a role that fits your background in Everest Clinical Research's listings on Migrate Mate, then follow the link through to Everest Clinical Research's own careers page to submit your application directly. Everest Clinical Research manages its own hiring process, including screening, interviews, and offers. Migrate Mate does not collect applications or charge candidates any fee to apply.
What do Everest Clinical Research jobs pay?
Listed salaries for Everest Clinical Research roles on Migrate Mate range from about $90,000 to $200,000 per year as of July 16, 2026, with most postings at manager level or above. Exact pay is set by Everest Clinical Research and shown on each listing.
Does Everest Clinical Research hire entry-level?
Most of Everest Clinical Research's open roles on Migrate Mate are manager level or above as of July 16, 2026. Entry-level openings are limited. Check individual Everest Clinical Research listings for stated experience requirements.
Where is Everest Clinical Research hiring?
Most Everest Clinical Research roles are based in Bridgewater, and about 100% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.