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Work Study Field Research Biologist Jobs in Raleigh, NC

Duke University

Research Technician I

Durham, NC

$20 - $27.02/hr

Work closely with the Principal Investigator to review assignments, analyze experimental results ... Biology, Zoology, Psychology, Botany, or another science-related field. Experience No additional ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

We take our work personally, we do it with empathy and we're committed to making a difference. Name ... field of study. Experience requirements: 3 years of experience in clinical research. Or ...

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Showing results 21-40

All JobsWork Study Field Research Biologist JobsWork Study Field Research Biologist Jobs in Raleigh, NC

Work Study Field Research Biologist information

See Raleigh, NC salary details

$35.5K

$85.4K

$129.3K

How much do work study field research biologist jobs pay per year?

As of Aug 21, 2026, the average yearly pay for work study field research biologist in Raleigh, NC is $85,379.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $99,600.00 per year, depending on experience, location, and employer.

What is the difference between Work Study Field Research Biologist vs Field Technician?

AspectWork Study Field Research BiologistField Technician
Required CredentialsTypically requires a bachelor's degree in biology, ecology, or related field; some roles may prefer or require a master's degreeOften requires a high school diploma or associate degree; some positions may prefer technical certifications
Work EnvironmentField research sites, laboratories, academic institutions, government agenciesField sites, environmental agencies, research facilities
Employer & Industry UsageUniversities, research institutions, government agencies, environmental organizationsEnvironmental consulting firms, research organizations, government agencies

The Work Study Field Research Biologist typically has more advanced education and engages in designing studies and analyzing data, whereas the Field Technician focuses on data collection and fieldwork support. Both roles are essential in ecological research but differ in responsibilities and qualifications.

What are the most commonly searched types of Field Research Biologist jobs in Raleigh, NC?

The most popular types of Field Research Biologist jobs in Raleigh, NC are:

Work Study Field Research Biologist jobs near you

Senior Clinical Research Associate

Parexel

Raleigh, NC • On-site

Full-time

Posted 11 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 74 rated research

Job description

Name of Employer: Parexel International LLC
Position Title: Sr. Clinical Research Associate
*Multiple Openings Available*
Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609
*100% Remote reporting to Raleigh, NC.
Hours: Full Time / 40 hours per week
Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported data. Represent the company at assigned clinical trial sites and be accountable for quality and delivery from site identification to the close of trial. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments. Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring, Termination Visits, and Site Motivational Visits, and generate site visit reports. Develop strategy to configure, distribute, and collect, review, and approve high-quality country-specific and site-specific documents, essential regulatory documents, and updated or amended regulatory documentation. Customize, review, and negotiate country/site-specific Informed Consent Forms, translations, and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA applications, resolve conflicts, and determine appropriate follow-up until receipt of final approval. Address and resolve issues at clinical trial sites, including the need for additional training, potential deficiencies in documentation, and communication. Follow-up on Case Report Form data entry, query status, and Serious Adverse Events. Assess and manage test article/study supply including supply, accountability, and destruction/return status. Review and follow-up on site payment status and ensure site receives payments on a timely manner. Communicate study issues that require immediate action with a proposed strategy for resolution. Ensure assigned sites are audit-ready and inspection-ready. Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring visits. Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol Guidelines. Guide Administrative Support Team members, review work, and provide feedback to the manager regarding performance.
Education requirements: Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 3 years of experience in clinical research.
Or, alternatively:
Education requirements : Master's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 1 year of experience in clinical research.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site Management and application of clinical trial methodology and terminology; Independently monitoring visits (Qualification, Site Initiation, and Monitoring); Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; and Communicating results to stakeholders in non-technical language.
Travel requirements: Up to 75% Domestic Travel.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #ES2401 to openings@parexel.com

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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