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Contract Biotech Clinical Research Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Wake Research

Clinical Research Coordinator

Dallas, TX

$24 - $32/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Wake Research

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Adecco

Clinical Research Associate

Waltham, MA · On-site

$32 - $33.75/hr

Temporary / Contract Schedule: Full-Time | Onsite Pay Rate: $32.00-$33.75 per hour Job Summary We ... Clinical research or pharmaceutical/biotechnology experience. * Experience with clinical sample ...

M3 Wake Research, Inc.

$60 - $80/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Required Qualifications Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. 0-3 years of experience in clinical research or clinical ...

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Contract Biotech Clinical Research information

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How much do contract biotech clinical research jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for contract biotech clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

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

AspectContract Biotech Clinical ResearchClinical Research Associate
CredentialsTypically requires a degree in life sciences, certifications like CCR or RAC beneficialRequires a degree in life sciences; certifications like CCR often preferred
Work EnvironmentContract-based, project-specific, often in biotech or pharmaceutical companiesUsually employed by CROs or sponsors, monitoring clinical trials at sites
Employer & IndustryBiotech firms, pharmaceutical companies, contract research organizationsPharmaceutical companies, CROs, biotech firms

Contract Biotech Clinical Research professionals focus on specific projects within biotech or pharma companies, often working on trial design and management. Clinical Research Associates primarily monitor clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What cities are hiring for Contract Biotech Clinical Research jobs?

Cities with the most Contract Biotech Clinical Research job openings:

What are the most commonly searched types of Biotech Clinical Research jobs?

The most popular types of Biotech Clinical Research jobs are:

What states have the most Contract Biotech Clinical Research jobs?

States with the most job openings for Contract Biotech Clinical Research jobs include:

Contract Biotech Clinical Research jobs near you

Clinical Research Coordinator

Dallas, TX • On-site

Winaxis
IT Services • 11 - 50 employees
Learn more about Winaxisexternal

$24 - $32/hr

Full-time

Re-posted 24 days ago

Job description

Job Summary: The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements. The role involves participant recruitment, study documentation, data collection, and ensuring the smooth execution of research activities while safeguarding participant safety and data integrity. Key Responsibilities: Coordinate and oversee day-to-day activities related to assigned clinical studies. Review study protocols and ensure all trial activities are conducted in compliance with protocol requirements. Recruit, screen, and enroll eligible study participants according to inclusion and exclusion criteria. Obtain and document informed consent from study participants prior to study procedures. Schedule participant visits and coordinate study assessments, procedures, and follow-ups. Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study records. Monitor participant safety by identifying, documenting, and reporting adverse events and serious adverse events in accordance with regulatory timelines. Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs), laboratory personnel, and other study stakeholders. Prepare for and support sponsor monitoring visits, audits, and regulatory inspections. Ensure adherence to Good Clinical Practice (GCP), institutional policies, and applicable local and international regulations. Track study timelines, recruitment targets, and protocol milestones. Assist with study initiation, amendments, close-out activities, and archiving of study documents. Maintain confidentiality of participant information and research data at all times. Required Qualifications: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred. Certification in Good Clinical Practice (GCP) is an advantage. Required Skills: Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal and written communication abilities. Attention to detail and accuracy in documentation. Proficiency in Microsoft Office applications and EDC systems. Ability to work independently and collaboratively within multidisciplinary teams. Effective problem-solving and interpersonal skills. Working Conditions: Work is typically performed in hospitals, research institutions, academic medical centers, or clinical research organizations. May require flexibility to accommodate participant schedules and sponsor visits.