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Clinical Research Remote Ophthalmology Jobs (NOW HIRING)

ClinChoice

Senior Clinical Research Associate

This is a permanent, fully remote position. Candidates must be willing and able to travel to ... Guide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.

ClinChoice

Senior Clinical Research Associate

This is a permanent, fully remote position. Candidates must be willing and able to travel to ... Guide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

  • Medical

  • Retirement

... ophthalmology, rare diseases, and neuroscience. Through our two business units- Emmes, a full ... conducts remote and on-site monitoring visits such as qualification pre study visits, site ...

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Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... ZH1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the ...

Tufts Medicine

$26.50 - $35.25/hr

The Clinical Research Coordinator II will support participant recruitment, study operations, data collection, regulatory compliance, and participant retention across clinic-based and remote research ...

Icon plc

Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Remote #LI-ZH1 Employment with ICON is contingent upon having the legal right to work in the ...

The Pennsylvania State University

$54K - $78K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... The Clinical Research Coordinator provides operational oversight for research projects and ...

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How much do clinical research remote ophthalmology jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical research remote ophthalmology in the United States is $30.16, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $31.97 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical research remote ophthalmology, and why are they important?

To thrive as a Clinical Research Remote Ophthalmology professional, you need a background in ophthalmology, clinical research methodologies, and familiarity with regulatory compliance, often supported by a relevant degree and experience in clinical trials. Experience using electronic data capture (EDC) systems, telemedicine platforms, and certifications such as GCP (Good Clinical Practice) are highly valuable. Strong communication, attention to detail, and self-discipline are essential soft skills for managing studies remotely and liaising with diverse teams. These skills ensure accurate data collection, regulatory compliance, and effective collaboration in a remote research environment.

What is a clinical research remote ophthalmology?

A Clinical Research Remote Ophthalmology job involves conducting ophthalmic research studies remotely, focusing on eye diseases, treatments, and clinical trials. Professionals in this role analyze patient data, collaborate with clinical teams, ensure regulatory compliance, and assist in study design. They may also manage documentation, monitor trial progress, and support data collection. This position typically requires a background in ophthalmology, clinical research, or a related field, along with strong analytical and communication skills.

What does a typical workday look like for someone in clinical research remote ophthalmology?

A typical workday in Clinical Research Remote Ophthalmology involves monitoring ophthalmic clinical trials, reviewing patient data, coordinating with investigators, and ensuring study protocols are followed—all from a remote location. You’ll often use digital platforms to track trial progress, report adverse events, and communicate regularly with site coordinators and research teams through email or video calls. Tasks may include data validation, regulatory documentation, and virtual site visits. This remote setting requires excellent organizational skills and proactive communication to maintain study quality and compliance while collaborating with team members across different time zones.

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What cities are hiring for Clinical Research Remote Ophthalmology jobs?

Cities with the most Clinical Research Remote Ophthalmology job openings:

What states have the most Clinical Research Remote Ophthalmology jobs?

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

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

The top searched job categories for Clinical Research Remote Ophthalmology jobs are:

Clinical Research Remote Ophthalmology jobs near you
Infographic showing various Clinical Research Remote Ophthalmology job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% Remote job distribution, with an average salary of $62,726 per year, or $30.2 per hour.

Senior Clinical Research Associate

ClinChoice

Remote

Full-time

Posted 4 days ago

Job description

ClinChoice is a global, full-service CRO providing clinical research services to pharmaceutical, biotechnology, medical device and consumer health companies. We are currently seeking an experienced Senior Clinical Research Associate (Senior CRA) to join our in-house team.
As a Senior CRA, you will manage 2-3 clinical trials and be responsible for site management activities, including study start-up, site monitoring, and closeout. You'll conduct both on-site and remote monitoring while supporting a variety of studies across a diverse client portfolio, from emerging biotech companies to large pharmaceutical organizations.
This is a permanent, fully remote position. Candidates must be willing and able to travel to investigative sites as needed.
Candidates must have experience monitoring oncology and other complex clinical trials, as well as previous experience working for a CRO. A strong understanding of GCP, ICH guidelines, and clinical trial operations is also required.
Join our team: you can be part of making a difference in people's lives and experience a fulfilling and rewarding career!
This is a remote role, ideal locations are West Coast, Northeast and/or Florida.
Main Job Tasks and Responsibilities:
  • Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.
  • Assist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by obtaining pre-study documentation to ensure good start-up of the investigation sites.
  • May act as Feasibility Associate.
  • Train site staff in all study procedures.
  • Conduct periodic monitoring visits, including completion of monitoring visit report. Review at each visit the accuracy, legibility, completeness and quality of the Case Report Forms (CRF).
  • Conduct source data verification and in-house review of clinical data and ensure timely resolution of data queries to guarantee reliable clinical data.
  • Manage the investigational products (storage, inventory, dispensing records, packaging and labelling) and the trial material (Investigator Study File (ISF), CRF, questionnaires, diaries, etc.) to ensure timely and correct supply to the site.
  • Cooperate with the site staff to ensure proper reporting from the site for safety issues (AEs, SAEs, SUSARs, etc.) and their follow-up, guaranteeing timely and appropriate handling of safety issues.
  • Conduct and report study termination and related activities (e.g. archiving) guaranteeing smooth completion of the project.
  • Act as the main contact person for the site to ensure close follow up.
  • Provide general support to the Clinical Research Division on quality control of clinical data.
  • Address appropriate team members about any issues that can jeopardise the conduct of the clinical projects assigned in a timely manner.
  • Report to the Head of department on all activities performed during the study and send all relevant documents according to the timelines and the requirements agreed for each single clinical trial.
  • Develop training material and give training in collaboration with the Training & Qualification Management Unit.
  • May assist with contract negotiation with sites on study budget after appropriate training.
  • Assist with the preparation of the study, including CRF design/development, write CRF instructions and organise the study files and documents to ensure good start-up of the investigation sites.
  • May support the submission process in the project including submission requirements, timelines, informed consent development, etc..
  • Guide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.

Education, Experience and Skills:
  • University Degree in scientific, medical or paramedical disciplines.
  • Previous experience working for a CRO is required.
  • At least eight (8) years of clinical research experience, including proven experience as a Clinical Research Associate (CRA) performing on-site monitoring activities.
  • Experience with oncology, respiratory and complex trials is required.
  • Strong knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements.
  • Fluent in English and local language(s).
  • Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).
  • Willingness to travel

The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
  • Key words: Clinical Research Associate, CRA, Freelance, Permanent, CRO, Contract Research Organization, Outsourced, Outsourcing, Oncology, Monitoring, Early Phase Oncology Trials, Senior CRA, Oncology Clinical Trials, CAR T, Investigative Site Monitoring, On-site Monitoring, Remote Monitoring, 1.0 FTE, 70% Travel, 1099, Independent Contractor, GCP (Good Clinical Practice), ICH Guidelines, FDA Regulations, Regulatory Compliance, Clinical Trial Operations, Source Data Verification (SDV), Case Report Forms (CRFs), Data Query Resolution, Safety Reporting (AE, SAE, SUSAR), Investigational Product (IP) Management, Site Initiation Visits (SIV), Site Selection Visits (SSV), Close-Out Visits (COV), Feasibility Assessment, Site Management, Study Start-Up, Clinical Data Quality Control, Monitoring Visit Reports, Investigator Study File (ISF), Trial Master File (TMF), Clinical Study Documentation, Site Training, Study Budget Negotiation, Informed Consent Development, Submission Support, 8+ Years CRA Experience, Advanced Oncology Experience, Phase I Oncology Monitoring, Early-Phase Oncology Trials, CRO Experience, U.S.-Based CRA

#LI-VH #LI-Remote #Senior Clinical Research Associate # Permanent

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