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Vision Research Cro Jobs in Texas (NOW HIRING)

ELLIGO HEALTH RESEARCH INC

Site Team Leader

Austin, TX · On-site

Working closely with Regional Site Directors and other Research Operations leaders, this individual ... CRO staff · Support business development and operations to achieve study awards · Providing ...

OptiSigns Inc.

Chief Revenue Officer

Houston, TX · On-site

This is not a traditional enterprise-sales CRO role. OptiSigns has two meaningful growth motions: a ... AI handles research, drafting, testing, and repetitive execution while people own judgment and ...

OptiSigns Inc.

Chief Revenue Officer

Houston, TX · On-site

This is not a traditional enterprise-sales CRO role. OptiSigns has two meaningful growth motions: a ... AI handles research, drafting, testing, and repetitive execution while people own judgment and ...

OptiSigns Inc.

Chief Revenue Officer

Houston, TX · On-site

$350 - $650/hr

AI handles research, drafting, testing, and repetitive execution while people own judgment and ... Vision insurance * Unlimited flexible aid time off * 401K Why OptiSigns You will inherit a ...

OptiSigns Inc.

Chief Revenue Officer

Grapeland, TX · On-site

This is not a traditional enterprise-sales CRO role. OptiSigns has two meaningful growth motions: a ... AI handles research, drafting, testing, and repetitive execution while people own judgment and ...

OptiSigns Inc.

Chief Revenue Officer

Houston, TX · On-site

This is not a traditional enterprise-sales CRO role. OptiSigns has two meaningful growth motions: a ... AI handles research, drafting, testing, and repetitive execution while people own judgment and ...

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Senior Clinical Scientist

Dallas, TX

... clinical research organisation united by a mission to bring new medicines and treatments to ... Participate in project teams and serve as liaison to project teams, CRO's, Clinical sub-teams, and ...

410 ICR United States USA

Lead CRA

Dallas, TX · On-site

Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO ... Health and wellbeing programmes including medical, dental, and vision coverage where applicable

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Lead CRA

Houston, TX · On-site

Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO ... Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Icon plc

Lead CRA

Dallas, TX · On-site

Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO ... Health and wellbeing programmes including medical, dental, and vision coverage where applicable

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Showing results 21-40

All JobsVision Research Cro JobsVision Research Cro Jobs in Texas

Vision Research Cro information

What is the difference between Vision Research Cro vs Vision Research Coordinator?

AspectVision Research CroVision Research Coordinator
CredentialsTypically requires a background in clinical research, regulatory knowledge, and industry-specific certificationsRequires similar research experience, often with additional project management or coordination certifications
Work EnvironmentWorks with CRO teams, clinical trial sites, and sponsors in a regulated industry settingCoordinates clinical trial activities at sites, liaising between investigators and sponsors
Employer & Industry UsageHired by pharmaceutical or biotech companies, CROs, and research organizationsEmployed by research sites, hospitals, or clinical research organizations

While both roles involve clinical research in the vision industry, a Vision Research Cro focuses on managing and overseeing clinical trials for sponsors, whereas a Vision Research Coordinator handles the day-to-day coordination at trial sites. Understanding these differences helps in choosing the right career path or job search focus.

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Vision Research Cro jobs near you

Round Rock -Clinical Research Coordinator I

Austin Retina Associates

Round Rock, TX • On-site

$22.50 - $30/hr

Full-time

Re-posted 22 days ago

Austin Retina Associates rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Clinical Research Coordinator I
Position Summary
Our goal is to advance retinal research, offer new treatment opportunities to our community, and provide the highest quality patient care. Austin Retina Associates is seeking a responsible, self motivated, individual to provide research coordination in a thriving retina practice's growing research department. Our ideal candidate is passionate about patient care and the administrative aspects of clinical research.
Duties/Responsibilities
  • Performs required trainings and obtains applicable certifications necessary to participate in specific study protocols including GCP, IATA, and other protocol-specific training
  • Facilitates and coordinates daily clinical trial activities
  • Primary coordinator on 1+single site studies within the practice
  • Ensure study staff are trained on study protocols, ICF, manuals and document all trainings
  • Will create, manage and maintain source documents for each assigned trial
  • Attend teleconferences and meetings as requested by research manager
  • Review and understand all study protocols including proceedings, timeline, inclusion/exclusion criteria, confidentiality and privacy protections
  • Provide care for study patients during visits, perform diagnostic testing,

schedule appointments and educate patients regarding retinal condition, available treatment
options and details of study protocol
  • Preview with patient the involvement of potential study and complete both physician and patient consent
  • Provide ongoing communication regarding study to patient's physicians
  • Perform data entry in multiple Electronic Data Capture, EDC, systems
  • Primary contact for monitor site visits, preparing documentation, and making corrections to meet requirements and deadlines as needed
  • Communicate and coordinate with study sponsor, monitors, and CRO's including data entry queries, audits and monitoring visits
  • Performs multiple imaging procedures required for specific study protocols; to be certified in digital imaging reading centers as utilized by each study sponsor
  • Manages and maintains all regulatory information about the study including protocols, investigator brochure, IRB documents, Investigator disclosures, CVs, training, documentation, instructions and reporting requirements for the IRB and the sponsor
  • Collects updated medical history, ALL adverse and serious adverse events and reports to the sponsor and IRB within the required timeframes
  • Screens patients for eligibility using protocol-specific inclusion and exclusion criteria,

documenting each potential participant's eligibility accurately
  • Other duties assigned on an as needed basis delegated by study protocol or manager
Required Attributes
  • Perform multiple imaging procedures required for each specific study protocol with the intent to be certified through the digital imaging reading center utilized by each study sponsor
  • Train and certify to perform refraction and vision testing
  • Deliver safe and appropriate care to patients in addition to the requirements outlined in Study

protocol, Good Clinical Practice (GCP) Guidelines, and Standard Operating Procedures (SOPs)
  • Ability and willingness to perform venipunctures and process samples with training provided
  • Master multiple computer systems including Google, MicrosoftOffice, Teams, data management
  • Ability to develop and maintain strong relationships with physicians, coworkers, and patients
  • Will master ophthalmology and retina terminology
  • ICH GCP Training/Certification
  • Certified Ophthalmic Assistant
  • Cooperates with supervisory staff, physicians, peers, external customers, and patients in a

positive, energetic, and professional manner
Preferred Attributes
  • Demonstrated effectiveness showing courtesy, diligence, integrity, and teamwork in alignment with ARA core values
  • Excellent organizational and time management skills ensuring all tasks are completed in a timely manner satisfactory to the organization with ability to independently manage workflow
  • Strong interpersonal skills including effective listening, clear communication, effective customer problem resolution with warm encouraging demeanor
  • Bilingual in Spanish
  • Ophthalmic experience
  • Demonstrates high-level initiative and critical thinking skills
  • College degree preferred, significant relevant experience, and/or Ophthalmic experience
  • CRA tier III and/or 18 months with prior performance review or assessment exceeding expectations
  • Experience in the following is preferred but not required: FA, FP, FAF, and IR imaging on

OIS/Topcon, Heidelberg and Optos, SD-OCT scanning on Heidelberg and Cirrus systems
  • CCRP or CCRC Certification
  • Experience with Real Time CTMS
Position Details
  • Schedule approximately 8-5pm during weekdays
  • Hourly pay, FLSA non-exempt, eligible for overtime

Physical Demands and Requirements
Prolonged standing and walking, some sitting, talking and hearing both in person and by telephone; use hands to finger, handle and feel objects or controls; reach with hands and arms. Regularly required to stoop, kneel, bend, crouch and lift up to 40 pounds on occasion. Specific vision abilities required by this job includes viewing multiple computer screens, close vision, distance vision, depth perception, color vision and the ability to adjust focus. Viewing images and operating computer devices constantly.

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