ZipRecruiter

Log In

1

Contract Biotech Clinical Research Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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 trial coordination.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/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 ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

previous page

Showing results 41-60

All JobsClinical Research JobsBiotech JobsFreelance JobsContract Biotech Clinical Research Jobs

Contract Biotech Clinical Research information

See salary details

$12

$41

$69

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

Medical, PTO

Re-posted 24 days ago

Job description

Job Title : Clinical Research Coordinator (CRC)

Experience : 0–3 Years

Location : Dallas, Texas

Employment Type : Full-time

Job Summary:-

We are looking for a motivated and detail-oriented Clinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate should have 0–3 years of experience in clinical research and a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Fresh graduates with relevant internships or clinical research training are encouraged to apply.

Key Responsibilities

  • Coordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations.

  • Screen, recruit, and enroll study participants.

  • Obtain informed consent from study participants.

  • Schedule and coordinate patient visits and follow-up appointments.

  • Collect, verify, and maintain accurate study documentation and source data.

  • Enter clinical data into Electronic Data Capture (EDC) systems.

  • Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents.

  • Report adverse events and serious adverse events according to protocol and regulatory requirements.

  • Coordinate with investigators, sponsors, CROs, and ethics committees.

  • Prepare for monitoring visits, audits, and regulatory inspections.

  • Ensure protocol compliance and participant safety throughout the study.

  • Assist with study start-up, close-out activities, and regulatory submissions.

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 trial coordination.

  • Knowledge of ICH-GCP, FDA, and local regulatory guidelines.

  • Familiarity with EDC systems and Microsoft Office.

  • Strong organizational, communication, and documentation skills.

  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications

  • GCP Certification.

  • Clinical Research certification is an added advantage.

  • Experience with site coordination or patient recruitment.

  • Knowledge of clinical trial documentation and regulatory submissions.

Key Skills

  • Clinical Trial Coordination

  • ICH-GCP Compliance

  • Patient Recruitment

  • Informed Consent Process

  • Source Documentation

  • Electronic Data Capture (EDC)

  • Trial Master File (TMF)

  • Regulatory Documentation

  • Adverse Event Reporting

  • Data Management

  • Communication & Coordination

  • Attention to Detail

  • Time Management

Benefits

  • Competitive salary

  • Health insurance

  • Performance-based incentives

  • Training and career development opportunities

  • Paid leave and holidays

  • Exposure to global clinical research projects

How to Apply

Interested candidates can submit their updated resume along with a cover letter highlighting their clinical research experience, certifications, and relevant skills.