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Summer Clinical Research Jobs (NOW HIRING)

$90 - $150/hr

Senior Clinical Research Associate (CRA) - Animal Health As a Senior Clinical Research Associate ... Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) * 8-week parental ...

Supervise summer students/interns and contribute to the training of Level I and new Level II ... Master's Degree preferred * 3-5 years of experience in clinical research * CCRP certification

$35/hr

Accompany Clinical Research Associate to monitor clinical data at clinical investigative sites * Prepare literature review summaries for comprehensive evaluation of current clinical outcomes in ...

New

$35/hr

Accompany Clinical Research Associate to monitor clinical data at clinical investigative sites * Prepare literature review summaries for comprehensive evaluation of current clinical outcomes in ...

New

Showing results 21-40

Summer Clinical Research information

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$13

$24

$40

How much do summer clinical research jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for summer clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a summer clinical research?

A Summer Clinical Research position is typically a temporary role offered to students or recent graduates who assist with medical or health-related research projects during the summer months. Participants may help with tasks such as data collection, patient recruitment, literature reviews, and administrative support under the supervision of experienced researchers. These internships provide valuable hands-on experience in clinical research settings, helping participants learn about the research process, ethics, and clinical trial protocols. It is an excellent opportunity for those interested in healthcare, medicine, or research careers to gain practical skills and professional connections.

What types of projects and responsibilities can I expect in a summer clinical research role?

In a summer clinical research position, you can expect to assist with a variety of research tasks, such as data collection, literature reviews, patient recruitment, and maintaining study documentation. You may also help coordinate with clinical staff and participate in weekly team meetings to discuss study progress. The role often involves learning standard research protocols and gaining exposure to ethical considerations in clinical trials. This hands-on experience is valuable for building foundational skills and networking with professionals in the clinical research field.

What are the key skills and qualifications needed to thrive in a summer clinical research role, and why are they important?

Success in a Summer Clinical Research role requires a solid understanding of scientific research methods, data analysis, and attention to detail, typically supported by coursework in biology, chemistry, or related fields. Familiarity with statistical software (like SPSS or R), electronic data capture systems, and compliance protocols such as IRB procedures is often expected. Strong communication, teamwork, and organizational skills help individuals stand out by facilitating collaboration and effective project management. These competencies ensure the accurate collection and analysis of data, adherence to ethical standards, and meaningful contributions to research outcomes.

What cities are hiring for Summer Clinical Research jobs?

Cities with the most Summer Clinical Research job openings:

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

The most popular types of Clinical Research jobs are:

What states have the most Summer Clinical Research jobs?

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

Senior Director, Clinical Research (Medical Director)

Eikon Therapeutics

Jersey City, NJ โ€ข On-site

$270K - $325K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Job description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position
We are seeking a physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician, Senior Director, Clinical Research. In this role, you will play a pivotal part in advancing our oncology and/or non-oncology pipeline by providing medical expertise, leadership, and operational oversight for a clinical development study(ies).
About You
You are a highly accomplished professional who excels in the development and execution of clinical projects. As a key member of the cross-functional Development Teams and the Clinical Study Teams, you will employ your expertise in clinical development to advance new therapies to patients in need. Your dedication to scientific rigor and meticulous attention to detail is evident in all your work. With a deep passion for creating important new medicines, you are committed to advancing the field of medical research and improving patient outcomes.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective collaboration and high-quality execution of your clinical work.
What You'll Do in partnership with your Manager
  • Design and conduct early-stage clinical development trials as needed, including, but not limited to assessing clinical safety and efficacy data, performing medical monitoring, and be responsible for other study-related clinical activities.
  • Interpret reports, and prepare oral and written results of product research.
  • Be proactive in fulfilling your responsibilities and pay particular attention to quality and accuracy of work as well as timeliness of deliverables.
  • Collaborate closely with relevant functions within Eikon including discovery, translational and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, and regulatory personnel.
  • Work closely with functional partners (Clinical Science, Data Management, Clinical Operations, Biostatistics) to ensure an integrated approach to flawless execution and systematic oversight of study protocol(s) in clinical development.
  • Work closely with functional partners to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion.

Qualifications
  • MD or DO degree with significant experience in Oncology.
  • Minimum of 5-7 years of clinical experience, including 3+ years in drug development.
  • Experience in clinical practice with direct patient care.
  • Proven track record in leading clinical trials, including medical monitoring of early and late stage clinical trials.
  • In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
  • Ability to work effectively in a matrixed environment.
  • Strong analytical, organizational, and problem-solving skills.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  • Passion for clinical trials and improving patient outcomes.
  • Experience with IND and/or NDA/BLA filings is preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $270,000 to $325,500 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.