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Ms Clinical Research Jobs (NOW HIRING)

Medtronic

Clinical Research Specialsit

Plymouth, MN

In this exciting role as a Clinical Research Specialist (CRS), you will be responsible for ... Proficiency in MS Office applications: Excel, PowerPoint and Word, Project (or similar scheduling ...

Medtronic

Clinical Research Specialsit

Plymouth, MN · On-site

In this exciting role as a Clinical Research Specialist (CRS), you will be responsible for ... Proficiency in MS Office applications: Excel, PowerPoint and Word, Project (or similar scheduling ...

Medtronic

Clinical Research Specialsit

Plymouth, MN · On-site

In this exciting role as a Clinical Research Specialist (CRS), you will be responsible for ... Proficiency in MS Office applications: Excel, PowerPoint and Word, Project (or similar scheduling ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Proficient with MS Office and EDC systems; willing to travel up to 80% * Ability to remain in a ...

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Ms Clinical Research information

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$49K

$107.3K

$189K

How much do ms clinical research jobs pay per year?

As of Jun 22, 2026, the average yearly pay for ms 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 the difference between Ms Clinical Research vs Clinical Research Coordinator?

AspectMs Clinical ResearchClinical Research Coordinator
Required CredentialsBachelor's or Master's in health sciences, clinical research certification often preferredBachelor's degree, certification optional but beneficial
Work EnvironmentResearch institutions, pharmaceutical companies, hospitalsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in academic, industry, and clinical research settingsPrimarily in clinical trial sites and hospitals
Common Search & ComparisonOften compared for research roles, data management, and study coordinationCompared for trial management, patient interaction, and data collection

The Ms Clinical Research role typically involves overseeing clinical studies, data analysis, and research design, often requiring advanced degrees. The Clinical Research Coordinator focuses on managing daily trial activities, patient coordination, and data collection at clinical sites. Both roles are essential in the research process but differ in scope and responsibilities.

What cities are hiring for Ms Clinical Research jobs? Cities with the most Ms Clinical Research job openings:
What states have the most Ms Clinical Research jobs? States with the most job openings for Ms Clinical Research jobs include:
Ms Clinical Research jobs near you
Infographic showing various Ms Clinical Research job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 4% As Needed, 89% Full Time, 5% Part Time, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

Medical Center Ophthalmology Associates

San Antonio, TX • On-site

$21 - $27.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

Company Overview
Medical Center Ophthalmology Associates located in San Antonio Texas offers compassionate care for every eye condition.(MCOA) Board certified physician's offer comprehensive eyecare their team is totally dedicated to help you see better.
Position Summary
Medical Center Ophthalmology Associates (MCOA), in San Antonio, TX, is now hiring an enthusiastic Clinical Research Coordinator to join our growing team. The Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator, and the Research Director. The team member will implement and coordinate research and administrative procedures for the successful management of clinical trials.
Responsibilities
A CRC is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.
  • Administratively and clinically manage 5-7 concurrently running clinical research trials, including data collection, data query response, and issue resolution within a timely manner.
  • Identify adverse events and report per protocol guidelines.
  • Assist in the planning and design of source documents for study protocols.
  • Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.
  • Provide patient care, not limited to but including greeting patients in a friendly and prompt manner, responding within appropriate time frame to patient questions and communications, escorting patients to exam rooms, verifying patient information, making necessary documentation within patient charts, discussing study protocols with patients, and ensuring correct informed consent is documented.
  • Work closely with physicians and doctors to update on changes in patient's health.
  • Administer topical ophthalmic or oral medications.
  • Maintain knowledge of operation and maintenance of clinical equipment, drugs, and supplies.
  • Discuss study protocols with patients and verify the informed consent documentation
  • Dispense study medication in a professional and accountable manner following protocol requirements
  • Collect, process, and ship blood/urine specimens at scheduled patient visits
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
  • Administer questionnaires/diaries per protocol.
  • Maintain HIPAA compliance for all patient information.
  • Adhere to all OSHA and Infectious Waste procedures.
  • Obtain reading center certification and perform ophthalmic imaging and special testing when applicable
  • Other duties as assigned.

Qualifications
Education and/or Work Experience Requirements:
• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research
• Analytical mindset
• Attention to detail
• Exceptional interpersonal skills
• Superior verbal and written communication skills
• Understanding of laboratory procedures and equipment
• Proficiency in MS Office - Word, Excel and Outlook
• High school diploma or equivalent GED
• Bilingual English/Spanish preferred.
Company Benefits
We offer a competitive benefits package to our employees:
  • Medical
  • Dental
  • Vision
  • 401k w/ Match
  • HSA/FSA
  • Telemedicine
  • Generous PTO Package

We also offer the following benefits for FREE:
  • Employee Discounts and Perks
  • Employee Assistance Program
  • Group Life/AD&D
  • Short Term Disability Insurance
  • Long Term Disability Insurance

EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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