ZipRecruiter

Log In

1

Eli Lilly Rn Jobs (NOW HIRING)

Oak St. Health

Registered Nurse

Freeport, NY · On-site

$72K - $155K/yr

Registered Nurse We're building a world of health around every individual -- shaping a more connected, convenient and compassionate health experience. At CVS Health ® , you'll be surrounded by ...

next page

Showing results 1-20

People also search for

All JobsEli Lilly Rn Jobs

Eli Lilly Rn information

See salary details

$9

$45

$93

How much do eli lilly rn jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for eli lilly rn in the United States is $45.47, according to ZipRecruiter salary data. Most workers in this role earn between $30.29 and $55.05 per hour, depending on experience, location, and employer.

What can I be instead of a nurse?

Eli Lilly Rn is a registered nurse role, but alternative careers include medical assistants, pharmacy technicians, clinical research coordinators, or healthcare administrators. These roles often require relevant certifications, knowledge of medical procedures, and familiarity with healthcare environments.

What does a typical workweek look like for an RN at Eli Lilly?

A typical workweek for an RN at Eli Lilly involves coordinating and monitoring clinical trial activities, supporting participant safety and protocol adherence, and collaborating closely with clinical research associates, physicians, and regulatory teams. You may be responsible for data collection, patient assessments, adverse event reporting, and ensuring compliance with regulatory standards. Regular meetings and cross-functional collaborations are common, and you will often need to adapt to evolving study demands. The environment is generally fast-paced and dynamic, providing exposure to cutting-edge medical research and opportunities to develop expertise in clinical trials.

Is it difficult to get a job at Eli Lilly?

Securing a position as an Eli Lilly RN can be competitive due to the company's reputation and industry standards. Candidates typically need relevant nursing experience, proper licensure, and may undergo multiple interview stages. Strong clinical skills and familiarity with healthcare regulations can improve chances of hiring.

What are the chillest nursing jobs?

For nurses, roles such as outpatient clinic nurse, school nurse, or telehealth nurse are often considered less stressful and have more predictable schedules. These positions typically involve regular hours, less emergency response, and a calmer work environment compared to hospital bedside nursing.

What are the key skills and qualifications needed to thrive in the Eli Lilly Rn position, and why are they important?

To excel as an Eli Lilly RN, you need a valid RN license, strong clinical nursing skills, and experience in pharmaceutical or clinical research settings. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) guidelines, and clinical trial protocols is commonly required. Excellent communication, attention to detail, and the ability to collaborate cross-functionally are important soft skills. These competencies ensure safe, compliant trial execution and effective coordination within multidisciplinary teams.

What are the typical salaries at Eli Lilly?

Eli Lilly RNs typically earn an average salary ranging from $70,000 to $90,000 annually, depending on experience, location, and certifications. Salaries for nursing roles at Eli Lilly can vary based on the specific position and level of responsibility, with some roles offering additional benefits such as bonuses and health insurance.

What is an Eli Lilly RN job?

An Eli Lilly RN (Registered Nurse) job typically involves providing clinical support for pharmaceutical research, patient education, or drug development programs. RNs in this role may work on clinical trials, ensuring compliance with protocols and regulatory standards, or support healthcare providers in understanding Eli Lilly’s medications. They may also assist in patient outreach, safety monitoring, or training other healthcare professionals. This position often requires a strong nursing background, knowledge of pharmaceuticals, and excellent communication skills.

More about Eli Lilly Rn jobs
What cities are hiring for Eli Lilly Rn jobs? Cities with the most Eli Lilly Rn job openings:
What are the most commonly searched types of Eli Lilly Rn jobs? The most popular types of Eli Lilly Rn jobs are:
What states have the most Eli Lilly Rn jobs? States with the most job openings for Eli Lilly Rn jobs include:
What job categories do people searching Eli Lilly Rn jobs look for? The top searched job categories for Eli Lilly Rn jobs are:
Eli Lilly Rn jobs near you
Infographic showing various Eli Lilly Rn job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $94,568 per year, or $45.5 per hour.
Clinical Trial Associate

Clinical Trial Associate

Repertoire Immune Medicines

Cambridge, MA • On-site

$36.50 - $49.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Repertoire Immune Medicines is a clinical-stage biotechnology company harnessing the power of the human immune system to develop transformative therapies for cancer and autoimmune disease. Using its proprietary DECODETM platform—which maps the immune synapse between T cell receptors (TCRs) and their antigen targets—Repertoire translates unique biological insights into potent, targeted immune medicines. The company integrates deep protein engineering expertise and has established collaborations with several leading pharmaceutical companies, including Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer.
Repertoire is advancing a pipeline of TCR bispecific immunotherapies with the potential to address a broad range of cancers and autoimmune disorders. The company’s lead oncology program, RPTR-1-201, a TCR bispecific, is currently in a Phase 1/2 clinical trial across multiple solid tumor indications. Repertoire plans to advance additional TCR bispecific therapies into clinical trials over the next 12–18 months. The Clinical Trial Associate will play a central role in supporting these programs.Position SummaryRepertoire Immune Medicines is seeking a highly motivated Clinical Trial Associate (CTA) to join our Clinical Operations team and support the execution of early-phase oncology clinical trials. The CTA will provide critical operational support in execution of clinical trials across trial start-up, conduct, maintenance, and close-out activities. In this role, the CTA will work closely with the Director of Clinical Operations and the Clinical Trial Manager, cross-functional team members, CROs, vendors, and clinical sites to help ensure timely, high-quality operational execution of clinical trial activities in compliance with ICH-GCP, applicable FDA and global regulatory requirements, GDPR/HIPAA where relevant, and Repertoire SOPs.
The ideal candidate is detail-oriented, highly organized, proactive, and comfortable working in a fast-paced biotech sponsor environment, with experience supporting oncology and early-phase clinical trials preferred.
The successful candidate will also value a highly collaborative, in-person team culture and be expected to work on-site in our Cambridge office three or more days per week.Key Responsibilities
Clinical Trial Execution and Operational Support
  • Support operational full life cycle execution of early-phase oncology clinical trials in accordance with protocol requirements, ICH-GCP, applicable global regulations, and company SOPs.
  • Coordinate trial activities across multiple functional areas, CROs, vendors, and clinical sites to support timely execution of trial deliverables and milestones.
  • Identify operational issues, assess potential impact to trial timelines or compliance, and escalate risks or mitigation recommendations to Clinical Operations leadership as appropriate.
  • Support site activation, readiness for investigational product release, trial supply coordination, and issue resolution activities.
  • Maintain trial trackers, distribution lists, reports, and clinical systems.
  • Track trial progress, including key milestones, vendor deliverables, enrollment, monitoring activities, and trial action items.
Regulatory, Trial Master File (TMF), and Compliance Support
  • Manage, organize, and maintain trial documentation to support inspection readiness and perform TMF quality checks including identification and resolution of documentation gaps, inconsistencies, and compliance risks.
  • Support preparation, review, tracking, and maintenance of regulatory and IRB/IEC documentation in collaboration with internal and external stakeholders.
  • Support audit and inspection readiness activities, including document retrieval, issue tracking, and follow-up coordination.
  • Track protocol deviations, operational issues, and compliance concerns, including escalation of significant risks to trial leadership.
Cross-Functional Coordination and Trial Oversight
  • Serve as an operational contact for CROs, vendors, and clinical sites under the direction of Clinical Trial Manager.
  • Coordinate trial meetings, prepare agendas and minutes, document key decisions and action items, and support timely follow-up and resolution of operational priorities.
  • Support operational oversight of CRO and vendor deliverables, timelines, and issue escalation activities.
  • Coordinate exchange of trial information and materials across cross-functional stakeholders to support execution and inspection readiness.
  • Exercise independent judgment in prioritizing competing operational activities and managing multiple trial deliverables.
Qualifications
  • Bachelor’s degree in life sciences, health sciences, nursing, public health, or related field.
  • Minimum of 2 years of experience supporting clinical operations, clinical research, or clinical trial execution activities.
  • Working knowledge of ICH-GCP, FDA regulations, and clinical trial processes within a biotech, sponsor, CRO, or research environment.
  • Experience with clinical systems and tools such as eTMF, EDC, CTMS, Smartsheet, Box, and Microsoft Office applications.
  • Strong organizational, analytical, and problem-solving skills with demonstrated ability to prioritize competing activities and manage multiple deliverables.
  • Ability to identify operational risks, support issue resolution, and escalate quality or compliance concerns appropriately.
  • Strong communication and cross-functional collaboration skills with internal and external stakeholders.
  • Experience supporting oncology or early-phase clinical trials is preferred.
The base salary for this role ranges from $62,000 to $86,000 and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future.
 
Repertoire is committed to building an inclusive culture.  Much as the power of the immune system lies in the diversity of T and B cells, we believe our best work comes from a diverse workforce—and we are committed to pursuing that in all facets of the work experience.
Repertoire is proud to be an Equal Opportunity Employer.  

Recruitment & Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto.

Powered by JazzHR

o2iNhCDhfn