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Biotech Clinical Research Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

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.

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

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.

IQVIA

Clinical Research Coordinator

Jefferson City, MO

$35 - $42/hr

Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... biotechnology, biomedical engineering, or a health-related field of study. Experience requirements ...

IQVIA

Clinical Research Coordinator

Marietta, GA · On-site

$35 - $42/hr

Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

IQVIA

Clinical Research Coordinator

Union, SC · On-site

$35 - $42/hr

Clinical Research Coordinator - Union, SC Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

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Biotech Clinical Research information

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$49K

$107.3K

$189K

How much do biotech clinical research jobs pay per year?

As of Aug 22, 2026, the average yearly pay for biotech clinical research 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 is a biotech clinical research?

A Biotech Clinical Research job involves conducting and managing clinical trials to evaluate the safety and efficacy of new drugs, medical devices, or treatments developed by biotechnology companies. Professionals in this field ensure compliance with regulatory guidelines, collect and analyze clinical data, and collaborate with cross-functional teams such as scientists, medical professionals, and regulatory authorities. Their work helps bring innovative therapies to market, improving patient care and advancing medical science.

What are the key skills and qualifications needed to thrive in biotech clinical research?

To thrive in Biotech Clinical Research, you need a solid background in life sciences, clinical trial methodologies, and regulatory compliance, usually supported by a relevant degree such as biology, biochemistry, or pharmacology. Experience with data management systems, statistical analysis software, and certifications like GCP (Good Clinical Practice) are highly valued. Exceptional attention to detail, effective communication, and strong problem-solving abilities are important soft skills for success in this role. These skills ensure clinical trials are conducted accurately, ethically, and efficiently, supporting the advancement of safe and effective biotech products.

What are some common challenges faced by professionals in biotech clinical research?

Professionals in biotech clinical research often encounter challenges such as managing complex regulatory requirements, adapting to frequent protocol amendments, and coordinating among diverse teams across multiple sites. Ensuring high data quality and maintaining strict timelines can also be demanding, especially as studies progress and new discoveries emerge. However, the dynamic nature of the work offers continuous learning opportunities and the reward of contributing to groundbreaking scientific advancements. Team members typically collaborate closely with clinical monitors, project managers, and regulatory affairs specialists to ensure every aspect of the research process runs smoothly.

What does a biotech clinical research do?

A biotech clinical research professional designs, manages, and monitors clinical trials to evaluate the safety and effectiveness of new drugs or therapies. They ensure compliance with regulatory standards, collect and analyze data, and collaborate with healthcare providers and regulatory agencies throughout the development process.

What qualifications do you need to be a biotech clinical researcher?

Biotech clinical researchers typically need a bachelor's degree in a life science, such as biology, chemistry, or related fields. Many roles require experience with clinical trial protocols, data analysis, and familiarity with regulatory requirements; advanced positions may require a master's or doctoral degree. Certifications like Good Clinical Practice (GCP) training can also enhance qualifications.
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What cities are hiring for Biotech Clinical Research jobs?

Cities with the most 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 Biotech Clinical Research jobs?

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

What job categories do people searching Biotech Clinical Research jobs look for?

The top searched job categories for Biotech Clinical Research jobs are:

Biotech Clinical Research jobs near you
Infographic showing various Biotech Clinical Research 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.

Clinical Research Coordinator

Winaxis

Boston, MA • On-site

$26.25 - $35/hr

Full-time

Re-posted 16 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.