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Clinical Research Biotech Remote Jobs (NOW HIRING)

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 ...

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Clinical Research Biotech Remote information

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$49K

$107.3K

$189K

How much do clinical research biotech remote jobs pay per year?

As of Aug 30, 2026, the average yearly pay for clinical research biotech remote in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What does a clinical research biotech remote professional do?

A Clinical Research Biotech Remote professional manages and oversees clinical trials and research studies for biotech companies while working from a remote location. Their responsibilities typically include coordinating study protocols, ensuring regulatory compliance, collecting and analyzing data, and collaborating with investigators and other stakeholders virtually. By working remotely, these professionals use digital tools to monitor trial progress and maintain communication with research teams, sponsors, and regulatory bodies. Their work plays a crucial role in advancing new biotech therapies and medical technologies.

How does a clinical research biotech remote professional collaborate with cross-functional teams?

In a remote Clinical Research Biotech role, professionals frequently collaborate with cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics. Communication typically occurs via video conferences, collaborative platforms, and shared digital workspaces. Successful candidates should be comfortable navigating time zone differences and proactively sharing updates to ensure project milestones are met. Building strong virtual relationships and maintaining transparency are key to overcoming challenges and ensuring seamless trial execution.

What are the key skills and qualifications needed to thrive as a clinical research biotech remote professional?

To thrive as a Clinical Research Biotech professional working remotely, you typically need a background in life sciences, experience in clinical research methodologies, and familiarity with regulatory requirements such as GCP and FDA guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and remote collaboration tools is essential. Strong organizational skills, self-motivation, and effective virtual communication set top performers apart in remote environments. These abilities are crucial for ensuring regulatory compliance, maintaining data integrity, and collaborating efficiently across dispersed teams.

What is the difference between Clinical Research Biotech Remote vs Clinical Research Associate?

AspectClinical Research Biotech RemoteClinical Research Associate
CredentialsBachelor's degree in life sciences; certifications like CCRP or RACBachelor's degree in life sciences; often required certifications like CCRP
Work EnvironmentRemote, flexible locationTypically on-site or travel-based, but remote options are increasing
Employer & IndustryBiotech companies, pharmaceutical firms, CROsPharmaceutical companies, CROs, biotech firms
Job FocusSupporting clinical trials remotely, data management, regulatory complianceMonitoring 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.

More about Clinical Research Biotech Remote jobs

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:

Infographic showing various Clinical Research Biotech Remote job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Senior Clinical Research Associate

WEP Clinical

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago


Job description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.
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.