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Pharmaceutical Research Associate Jobs (NOW HIRING)

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Research Associate III

Portland, OR · On-site

$62K - $75K/yr

Position Title: Research Associate III Full Time, Exempt Employee Job Reference ID: 21306261 ... Our mission is to help biotech, pharmaceutical, and academic clients make discoveries important to ...

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare ... We advance clinical research by providing outsourced services to pharmaceutical, biotechnology ...

... a Research Associate, non-tenure track in the Department of Diagnostic Radiology and Nuclear ... Pharmaceutical Sciences, Toxicology, or a related field. * A minimum of three years post-doctoral ...

... a Research Associate, non-tenure track in the Department of Diagnostic Radiology and Nuclear ... Pharmaceutical Sciences, Toxicology, or a related field. * A minimum of three years post-doctoral ...

... a Research Associate, non-tenure track in the Department of Diagnostic Radiology and Nuclear ... Pharmaceutical Sciences, Toxicology, or a related field. * A minimum of three years post-doctoral ...

Hiring a Field Research Associate for one of the top Agriculture company's in Woodland, CA M-F day ... Experience working on market research initiatives in biotechnology, pharmaceutical, or healthcare ...

The Center for Drug Discovery, in association with the Bouve College of Health Sciences, Department of Pharmaceutical Sciences, and Professor Lei Xie seek to hire a Postdoctoral Research Associate to ...

Field Research Associate

Woodland, CA · On-site

$20 - $28/hr

Hiring a Field Research Associate for one of the top Agriculture company's in Woodland, CA M-F day ... Experience working on market research initiatives in biotechnology, pharmaceutical, or healthcare ...

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Pharmaceutical Research Associate information

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$16

$32

$46

How much do pharmaceutical research associate jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for pharmaceutical research associate in the United States is $32.54, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $37.02 per hour, depending on experience, location, and employer.

What are some common challenges faced by Pharmaceutical Research Associates when managing multiple clinical trials simultaneously?

Pharmaceutical Research Associates often juggle several clinical trials at once, which can present challenges such as coordinating timelines, ensuring regulatory compliance, and maintaining clear communication with cross-functional teams. Balancing the priorities of different studies, troubleshooting unforeseen issues, and adapting to evolving protocols require strong organizational and problem-solving skills. Effective time management and proactive collaboration with clinical monitors, data managers, and regulatory specialists are essential to successfully navigate these complexities and maintain high-quality research standards.

What is the difference between Pharmaceutical Research Associate vs Clinical Research Coordinator?

AspectPharmaceutical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree in life sciences, often with industry certificationsBachelor's degree in health sciences or related field, often with clinical research certifications
Work EnvironmentPharmaceutical companies, research labs, biotech firmsHospitals, clinics, research sites
Industry UsageDrug development, preclinical and clinical trials in pharmaOverseeing clinical trial processes at research sites
Job FocusAssisting in drug research, data collection, and analysisManaging patient recruitment, data entry, and trial coordination

The Pharmaceutical Research Associate primarily focuses on supporting drug development within pharmaceutical companies, while the Clinical Research Coordinator manages clinical trial activities at research sites. Both roles require similar educational backgrounds and certifications but differ in work environment and specific responsibilities.

What do pharmaceutical research associates do?

A pharmaceutical research associate conducts experiments and analyzes data to develop and evaluate new drugs or medical treatments. They work in laboratories, often using specialized tools and following strict regulatory guidelines, and typically require knowledge of scientific methods and attention to detail.

How to get a job in pharmaceutical research?

To get a job as a Pharmaceutical Research Associate, candidates typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, with many roles preferring a master's or Ph.D. for advanced positions. Relevant skills include laboratory techniques, data analysis, and familiarity with regulatory guidelines. Gaining experience through internships or research projects and obtaining certifications such as Good Laboratory Practice (GLP) can improve job prospects.

What does a pharmaceutical associate do?

A pharmaceutical research associate supports the development and testing of new drugs by conducting experiments, collecting data, and analyzing results in laboratory or clinical settings. They often use laboratory equipment, follow strict safety protocols, and may assist in preparing reports for regulatory submissions.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Research Associate, and why are they important?

To thrive as a Pharmaceutical Research Associate, you need a solid background in life sciences, chemistry, or pharmacology, often supported by a bachelor's or master's degree in a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) guidelines, and analytical instruments like HPLC or mass spectrometry is typically required. Strong attention to detail, critical thinking, and effective teamwork are essential soft skills for success in this role. These competencies ensure accurate data collection, regulatory compliance, and the efficient advancement of pharmaceutical research projects.

Is a research associate a good career?

A Pharmaceutical Research Associate is a valuable role in drug development and clinical trials, requiring strong analytical skills and knowledge of laboratory techniques. It offers opportunities for career growth, specialization, and involvement in innovative medical research. The position typically requires a relevant degree and may involve working in a regulated environment with adherence to safety and quality standards.

What does a Pharmaceutical Research Associate do?

A Pharmaceutical Research Associate is responsible for supporting clinical trials and research studies that help develop new medications and treatments. Their duties include collecting and analyzing data, ensuring compliance with regulatory standards, and assisting with the documentation and reporting of research findings. They work closely with scientists, clinical investigators, and regulatory bodies to ensure the accuracy and integrity of research processes. This role is crucial in advancing medical knowledge and bringing new drugs to market safely and efficiently.
More about Pharmaceutical Research Associate jobs
What cities are hiring for Pharmaceutical Research Associate jobs? Cities with the most Pharmaceutical Research Associate job openings:
What are the most commonly searched types of Pharmaceutical Research jobs? The most popular types of Pharmaceutical Research jobs are:
What states have the most Pharmaceutical Research Associate jobs? States with the most job openings for Pharmaceutical Research Associate jobs include:
Infographic showing various Pharmaceutical Research Associate job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 8% Part Time, 1% Temporary, and 1% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $67,685 per year, or $32.5 per hour.
Senior Medical Research Associate

Senior Medical Research Associate

Icon plc

Lenexa, KS

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago


Job description

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Paramedic - PRN

Note: The internal title for a licensed paramedic at ICON is Senior Research Associate. Further details below.

ICON plc is a world-leading clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

The Role:

Our full-service clinic in Lenexa, Kansas, is a 114-bed, state-of-the-art research center, located near metropolitan Kansas City.

We are seeking a (PRN) Senior Medical Research Associate with active Paramedic licensure to support clinical research studies at our Lenexa, Kansas (KS) clinic.

Whether you're exploring a career in clinical research or already have experience in the field, this role offers a chance to contribute to work that supports the future of healthcare and disease management. Paramedic candidates without research experience are encouraged to apply.

Key Responsibilities

The Senior Medical Research Associate opportunity blends patient care with research responsibilities.

Clinical & Paramedic Responsibilities

  • Provide direct patient care within the onsite clinic, including advanced assessment, triage, vital signs, and urgent clinical support.

  • Perform Paramediclevel procedures within licensure scope, including IV placement, blood draws, specimen collection, injections, wound care, and emergency response/stabilization.

  • Monitor participant safety during research procedures and respond promptly to medical concerns, adverse events, or unexpected clinical situations.

  • Ensure medical equipment, supplies, and emergency materials are maintained, stocked, and fully operational.

Research & Operational Responsibilities

  • Assist in planning, coordinating, and executing clinical research activities in alignment with study protocols and regulatory requirements.

  • Support study visit procedures, including sample handling, documentation, timing, and protocoldriven tasks.

  • Conduct or support staff training, reinforce protocol adherence, and provide ongoing operational assistance to investigators and team members.

  • Track study progress, maintain accurate and auditready documentation, and ensure highquality records throughout the study lifecycle.

  • Contribute to the development and review of study materials, including source documents, manuals, logs, and operational tools.

Qualifications

  • Active, unrestricted Paramedic state license.

  • National Registry Paramedic (NRP) certification or staterecognized equivalent.

  • Strong understanding of patient assessment, emergency response protocols, and clinical documentation standards.

#LI-KM3


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply