The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...
The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...
Senior Clinical Research Associate (Pool)
CA · Remote
$120K - $145K/yr
This position is available for remote work in the following states: AZ, CA, CO, FL, GA, KS, KY, MA ... and biotechnology companies of all sizes in a variety of therapeutic areas. Our mission is to ...
Senior Clinical Research Associate (Pool)
CA · Remote
$120K - $145K/yr
This position is available for remote work in the following states: AZ, CA, CO, FL, GA, KS, KY, MA ... and biotechnology companies of all sizes in a variety of therapeutic areas. Our mission is to ...
Clinical Research Patient Recruiter - Remote
$23 - $25/hr
Clinical Research Patient Recruiter Remote | $23-$25/hour | Full-Time Are you confident on the phone and motivated by connecting with people? IMA Clinical Research is seeking an energetic, personable ...
Clinical Research Patient Recruiter - Remote
$23 - $25/hr
Clinical Research Patient Recruiter Remote | $23-$25/hour | Full-Time Are you confident on the phone and motivated by connecting with people? IMA Clinical Research is seeking an energetic, personable ...
Clinical Research Manager
Baltimore, MD · On-site +1
$55K - $97K/yr
The Clinical Research Manager works under the general supervision of a Pl(s) to manage the ... Remote Department name: SOM Neuro BIOS Personnel area: School of Medicine
Clinical Research Manager
Baltimore, MD · On-site +1
$55K - $97K/yr
The Clinical Research Manager works under the general supervision of a Pl(s) to manage the ... Remote Department name: SOM Neuro BIOS Personnel area: School of Medicine
Clinical Research Financial Analyst (Remote)
$70K - $80K/yr
Remote Essential Responsibilities: * Research and map clinical research financials via Advarra Visit Variation Report to contract pricing. * Collaborate with Sponsors and CROs to organize direct ...
Clinical Research Financial Analyst (Remote)
$70K - $80K/yr
Remote Essential Responsibilities: * Research and map clinical research financials via Advarra Visit Variation Report to contract pricing. * Collaborate with Sponsors and CROs to organize direct ...
Strong scientific and clinical research knowledge is required. * Strong understanding of clinical ... Ability to work efficiently in a remote and virtual environment. * Understand cultural inclusion.
Strong scientific and clinical research knowledge is required. * Strong understanding of clinical ... Ability to work efficiently in a remote and virtual environment. * Understand cultural inclusion.
Senior Clinical Research Associate
OR · Remote
$90K - $120K/yr
Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field. * 2-6 years of experience as a Clinical Research Associate in clinical trials. * Strong knowledge ...
Quick apply
Senior Clinical Research Associate
OR · Remote
$90K - $120K/yr
Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field. * 2-6 years of experience as a Clinical Research Associate in clinical trials. * Strong knowledge ...
... clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 ... Enjoy hybrid or remote working arrangements, depending on your location and role. • Career Growth
... clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 ... Enjoy hybrid or remote working arrangements, depending on your location and role. • Career Growth
Senior Clinical Research Associate
OR · Remote
$90K - $120K/yr
Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field. * 2-6 years of experience as a Clinical Research Associate in clinical trials. * Strong knowledge ...
Quick apply
Senior Clinical Research Associate
OR · Remote
$90K - $120K/yr
Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field. * 2-6 years of experience as a Clinical Research Associate in clinical trials. * Strong knowledge ...
... for our clients and advancing clinical research projects. As a part of the Global Project ... REMOTE
... for our clients and advancing clinical research projects. As a part of the Global Project ... REMOTE
Clinical Research Regulatory Specialist
Los Angeles, CA · On-site +1
Clinical Research Coordinator (eRegulatory Implementation Lead) University of Southern California ... Work hours and remote days may be subject to change depending on business needs. The annual range ...
Clinical Research Regulatory Specialist
Los Angeles, CA · On-site +1
Clinical Research Coordinator (eRegulatory Implementation Lead) University of Southern California ... Work hours and remote days may be subject to change depending on business needs. The annual range ...
Clinical Research Regulatory Specialist
Los Angeles, CA · On-site +1
Clinical Research Coordinator (eRegulatory Implementation Lead) University of Southern California ... Work hours and remote days may be subject to change depending on business needs. The annual range ...
Clinical Research Regulatory Specialist
Los Angeles, CA · On-site +1
Clinical Research Coordinator (eRegulatory Implementation Lead) University of Southern California ... Work hours and remote days may be subject to change depending on business needs. The annual range ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Chicago, IL · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Chicago, IL · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Miami, FL · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Miami, FL · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Houston, TX · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Houston, TX · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Nashville, TN · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Nashville, TN · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Boston, MA · On-site +1
... Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...
Clinical Research Biotech Remote information
See salary details
$49K - $61.7K
3% of jobs
$61.7K - $74.5K
13% of jobs
$79.6K is the 25th percentile. Wages below this are outliers.
$74.5K - $87.2K
22% of jobs
The median wage is $98K / yr.
$87.2K - $99.9K
14% of jobs
$99.9K - $112.6K
16% of jobs
$118.2K is the 75th percentile. Wages above this are outliers.
$112.6K - $125.4K
16% of jobs
$125.4K - $138.1K
7% of jobs
$138.1K - $150.8K
6% of jobs
$150.8K - $163.5K
2% of jobs
$163.5K - $176.3K
0% of jobs
$176.3K - $189K
0% of jobs
$49K
$107.3K
$189K
How much do clinical research biotech remote jobs pay per year?
What does a clinical research biotech remote professional do?
How does a clinical research biotech remote professional collaborate with cross-functional teams?
What are the key skills and qualifications needed to thrive as a clinical research biotech remote professional?
What is the difference between Clinical Research Biotech Remote vs Clinical Research Associate?
| Aspect | Clinical Research Biotech Remote | Clinical Research Associate |
|---|---|---|
| Credentials | Bachelor's degree in life sciences; certifications like CCRP or RAC | Bachelor's degree in life sciences; often required certifications like CCRP |
| Work Environment | Remote, flexible location | Typically on-site or travel-based, but remote options are increasing |
| Employer & Industry | Biotech companies, pharmaceutical firms, CROs | Pharmaceutical companies, CROs, biotech firms |
| Job Focus | Supporting clinical trials remotely, data management, regulatory compliance | Monitoring clinical trials, site visits, ensuring protocol adherence |
While both roles involve clinical trial support, Clinical Research Biotech Remote focuses on remote data and regulatory tasks within biotech companies, whereas Clinical Research Associate typically involves on-site monitoring and site management. The remote role offers flexibility, while the CRA role emphasizes direct site interaction.
What cities are hiring for Clinical Research Biotech Remote jobs?
Cities with the most Clinical Research Biotech Remote job openings:
What states have the most Clinical Research Biotech Remote jobs?
States with the most job openings for Clinical Research Biotech Remote jobs include:
What job categories do people searching Clinical Research Biotech Remote jobs look for?
The top searched job categories for Clinical Research Biotech Remote jobs are:
- Contract Senior Clinical Research Associate
- Clinical Research Remote Ophthalmology
- Remote Gsk Clinical Research
- Remote Merck Clinical Trials
- Remote Icon Clinical Research
- Remote Clinical Research Oncology
- Entry Level Clinical Data Manager
- Clinical Research Operations Manager
- Remote Clinical Research
- Remote Duke Clinical Research

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 13 days ago
Job description
Role Objectives:
The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs. They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready. The Senior CRA builds strong relationships with sponsors and sites, serving as a key point of contact throughout the study. They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.
Complex Study Experience Required
The Ideal Candidate:
- Leader
- Detail Oriented
- Problem Solver
- Adaptable
What You'll Do:
- Contribute to the design and review of study documents (protocols, CRFs, ICFs, and study plans).
- Lead site feasibility activities: distribute/collect questionnaires, evaluate responses, conduct SQVs, and recommend sites for selection.
- Planned and conducted SIVs, routine monitoring, and close-out visits in line with protocol, ICH-GCP, and regulatory requirements.
- Build strong relationships with site staff; deliver training and ongoing guidance on protocol compliance and regulations.
- Verify source data and CRFs for completeness, accuracy, and consistency; always keep site files audit-ready.
- Review IP accountability, safety event documentation, and protocol deviations; drive corrective and preventative actions.
- Manage and resolve data queries, analyze error trends, and provide targeted retraining to prevent recurrence.
- Track and close action items within study or company timelines; maintain clear oversight of monitoring deliverables.
- Support investigator meetings and key internal/external meetings; contribute to SOPs, monitoring tools, and templates.
- (Lead CRA, if assigned) Oversee monitoring on complex studies; develop study-specific monitoring documents (e.g., CMP, deviation plan, report templates); finalize visit reports; train/coordinate CRAs; act as primary clinical monitoring contact for PM/Sponsor and handle CRA escalations.
What You'll Need:
- Bachelor's degree (life sciences, nursing, or related field preferred)
- 5-7+ years' experience conducting on-site and remote monitoring visits (or equivalent clinical research experience)
- Senior CRA levelling: SCRA I (3-5 yrs) - independently manages complex sites; SCRA II (5+ yrs) - oversees complex sites/regions, mentors peers, and drives process improvements
- Broad therapeutic exposure across multiple study types and indications
- Strong technical/scientific aptitude with the ability to quickly grasp and execute clinical protocols
- Advanced organizational and logistical skills; able to manage multiple sites/protocols within budget and timelines
- Excellent written and verbal communication; confident stakeholder engagement
- Solid understanding of medical/therapeutic areas and medical terminology
- Proven ability to train, coach, and mentor clinical research staff
- Proficient with MS Office and EDC systems; willing to travel up to 80%
- Ability to remain in a stationary position for extended periods as part of normal day-to-day activities, with reasonable accommodations considered where appropriate
Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia.
What We Offer:
Medical, dental, and vision insurance
FSA, HSA
Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
Group short-term and long-term disability insurance
Group Life Insurance
401K safe harbor plan and company match
Paid vacation, holiday, sick and volunteer time
Paid maternity & paternity leave
What Sets Us Apart:
WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.
We're Committed to Our Team:
WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.
How We Work at WEP Clinical:
At WEP Clinical, we look for individualswho are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.
Our Services Include:
Access Programs
Clinical Trial Services
Patient Site Solutions
Clinical Trial Supply
Market Access and Commercialization
Data Privacy Notice:
WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.
Privacy Policy: https://www.wepclinical.com/privacy-policy/
Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn's Easy Apply option. Please ensure your resume is in English.
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.
For Your Safety, Please Note:
We will nevercommunicate with you via Microsoft Teams or text message
We will never ask for your bank account information at any stage of recruitment
WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.
WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
#LI-fulltime #LI-remote
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About WEP Clinical
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Morrisville, NC, US
Year founded
2008