Top 5 Assistant clinical research coordinator Jobs in Oxnard Ca

Clinical Research Coordinator
California Retina Consultants —Oxnard, CA
- $25.50 - $31.50 an hour
- Full-time
- Background check
- Anatomy knowledge
- Pass drug screening
- Paid holidays
- Dental insurance
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5d
Assistant Clinical Research Coordinator
Om Research LLC —Camarillo, CA
- $16 - $25 an hour
- Spanish
- Teaching
- Entry level
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Physician Assistant - Clinical Trials
California Dermatology Institute —Thousand Oaks, CA
- $75 - $110 an hour
- Part-time
- CPR Certification
- Mid-level
- In-person
- Health insurance
- 401(k)
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9d
Now Hiring: Medical Coordinator, EMTS, CNAs or MAs ( $28.00 -$32.00/ HR Depending on Experience)
Good Samaritan Shelter —Ventura, CA
- $28 - $32 an hour
- Full-time
- Computer literacy
- Mid-level
- Microsoft Office
- Health insurance
- Dental insurance
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4d

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Physician Assistant - Clinical Trials
California Dermatology Institute —Thousand Oaks, CA
Current California Physician Assistant license. DEA license (or ability to obtain). Interest in clinical research and evidence-based medicine.
$75 - $110 an hour
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9d
Clinical Research Assistant- Medical Oncology- ** Spanish Speaking**
Valkyrie Clinical Trials —Los Angeles, CA
Complete research test results; collates data; performs statistical analysis of lab results and maintain notes and log or computer database; performs basic…
$39,000 - $50,000 a year
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Assistant Clinical Research Coordinator
Dermatologists of Central States —Canal Winchester, OH
Assist with data entry, coding, and analysis as needed. Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health).
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BPC Redaction Clinical Research Assistant
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…
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Clinical Research Coordinator

California Retina Consultants -
Oxnard, CA

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Job Details

Full-time
$25.50 - $31.50 an hour
5 days ago

Benefits

Paid holidays
Dental insurance
401(k)
Vision insurance
Life insurance

Qualifications

Anatomy knowledge
Laboratory inventory control
Informed consent
Tonometers
Adverse event reporting
Clinical incident reports
Team leadership
Patient assessment
Ophthalmology
Practice management software
Patient management software
Mid-level
ECG equipment
Patient safety
Research project coordination
ICH guidelines
Patient history taking
Clinical staff training
Records management
Bachelor's degree
Clinical data entry
Clinical training
Clinical staff mentoring
Team training
Informed consent procedures implementation
Managing clinical research teams
Research compliance clinical trial records management
Organizational skills
Clinical trial standard operating procedures
Clinical trial patient safety management

Full Job Description

Clinical Research Coordinator

Job Summary

The Clinical Research Coordinator is responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and / or manual of procedures. Day to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties / Responsibilities

Level I

Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Administer sponsor required questionnaires (i.e. VFQ).
Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand.
Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented.
Creates, manages, and maintains source documents for each trial.
Attends teleconferences and investigator meetings as requested by research director.
Reviews and comprehends all study protocols, e.g. study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals.
Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant’s eligibility accurately.
Efficiently completes all study tasks delegated to them (i.e. scribing, VFQ, IOP, etc.).
Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within the required timeframe.
Conducts and / or participates in the informed consent process / discussion with research participants, including answering any questions related to the study.
Assures that amended consent forms are appropriately implemented and signed.
Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately.
Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract.
Oversees data and ensures that it is being entered correctly and resolves any queries issued within the required timeframe. • Collects and reports ALL Adverse Events.
Collects and reports ALL Serious Adverse Events.
Responsible for ensuring all SUSAR / Safety Reports are acknowledged and reviewed.
Coordinates monitor site visits and assists with preparation of site visit documentation.
Works with the monitor site visits and assists with preparation of site visit documentation.
Works with the monitor to make any corrections needed to meet requirements and deadlines as needed.
Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and sponsor.
Obtain any applicable additional / required sponsor training and / or certifications.

Level II (in addition to Level I)

Primary coordinator for multi-site studies within the practice.
Primary sponsor lead for multi-sites within the practice.
Reviews in-depth medical and / or hospital records for Serious Adverse Events.
Is proficient in all aspects of the CTMS system (i.e. running reports).
Mentors and trains research assistants and study coordinators.

Level III (in addition to Level I & Level II)

Primary coordinator for multi-site studies within the practice.
Provides leadership to the team.
Travel to other RCA sites for mentoring and collaboration.
Mentors and trains research assistants and study coordinators within practice.

About the Candidate

Preferred Skills / Abilities

Efficiently and accurately interviews patients and documents histories.
Demonstrates working knowledge of eye anatomy, disease, symptoms, and ocular medications.
Accurately performs labs, ECG, tonometry, pupil exam, data entry, and other specified duties.
Possesses excellent organizational skills to independently manage workflow.
Pays meticulous attention to detail.
Takes initiative.
Possesses insight and energy to prioritize quickly.
Demonstrates high-level critical thinking skills.
Cooperates with supervisory staff, physicians, peers, external customers, and patients in a positive, energetic, and professional manner.
Demonstrates excellence in communication skills, both personal and written.
Abounds in organizational time-management skills.

Education and Experience

Level I

Bachelor's degree in a related field preferred; combined experience and education as a substitute for minimum education.
Ophthalmic experience preferred.
Experience as RA III for one to three years or prior annual review or promotion assessment exceeds expectations and shows high proficiency in the job requirements.
ICH GCP Training / Certification.
IATA Certification.

Level II

Level I Coordinator for more than one year.
Prior annual review or promotion assessment exceeds expectations and shows proficiency in the job requirements.

Level III

Level II Coordinator for more than one year.
Prior annual review or promotion assessment exceeds expectations and shows proficiency in the job requirements.
SOCRA / ACRP Certification.

Who We Are

California Retina Consultants (CRC) is part of Retina Consultants of America (RCA), the largest network of leading retina specialists with the mission of saving sight and improving patient lives through innovation and the highest quality care. Through RCA's physician-centered practice management model, physicians continue to drive clinical and practice culture while benefiting from the available business expertise, resources and shared best practices.

Benefits

Medical Insurance Plans
Vision Insurance Plan
Dental Insurance Plan
401K Contribution
Life Insurance
Sick, Vacation, and Holiday Pay
Certification Opportunities

Equal Opportunity Employer

California Retina Consultants is proud to be an Equal Employment Opportunity and an Affirmative Action Employer. We are committed to creating an inclusive work environment that celebrates diversity.

All offers are contingent upon satisfactory background check and pre-employment drug screen.

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assistant clinical research coordinator jobs in oxnard ca

Clinical Research Coordinator

Assistant Clinical Research Coordinator

Physician Assistant - Clinical Trials

Now Hiring: Medical Coordinator, EMTS, CNAs or MAs ( $28.00 -$32.00/ HR Depending on Experience)

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