Top 13 training coordinator Jobs in rocklin, ca

Clinical Research Coordinator- Greenback
Retina Sacramento MSO LLC —Sacramento, CA
- $31.00 - $44.50 an hour
- Full-time
- Private practice
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Intake Coordinator Home Health
Compassionate Home Health Ltd —Roseville, CA
- $18 - $19 an hour
- Full-time
- HIPAA
- Office
- Administrative experience
- Health insurance
- 401(k)
Quick Apply
Patient Care Coordinator
Marina Milstein Orthodontics —Auburn, CA
- $19 - $28 an hour
- Part-time
- Private practice
- Dental office
- Customer service
- 401(k)
- Employee discount
Quick Apply
3d
Unit Secretary / Intake Coordinator
Dialysis Clinic, Inc. —Sacramento, CA
- $24 - $28 an hour
- 8 hour shift
- Word processing
- High school diploma or GED
- Clinic
- Paid training
- Wellness program
Quick Apply
Coordinator, Training and Administration
University Enterprises, Inc. —Sacramento, CA
- $4,432 - $6,648 a month
- 8 hour shift
- Background check
- English
- Mid-level
- Paid holidays
- Health insurance
Training Coordinator
WESTCARE CALIFORNIA INC —North Highlands, CA
- $26.50 - $27.78 an hour
- CPR Certification
- Management
- Current TB test
Quick Apply
11d
Quality & Training Coordinator (Sacramento)
Cambrian Homecare, Inc. —Sacramento, CA
- From $24.55 an hour
- Full-time
- Background check
- Spanish
- English
Sales and Marketing Coordinator
SafeSplash Sacramento —Sacramento, CA
- $21 - $22 an hour
- Weekends as needed
- Google Workspace
- Mid-level
- 1 year
- Paid training
- Employee discount
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Intake Coordinator Home Health
Compassionate Home Health Ltd —Roseville, CA
Reliable transportation and ability to travel to patient homes or field locations as needed. Assist with scheduling and coordinating home health visits for…
$18 - $19 an hour
Quick Apply
Lead Caregiver/Intake Coordinator
Golden Poppy Caregiving —Folsom, CA
Reliable transportation and valid driver’s license. Comfortable working in both home care environments and field settings. Train and mentor new caregivers.
$22 - $25 an hour
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3d

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Commercial Roofing Project Coordinator
Burns & Scalo Roofing Ohio —Columbus, OH
Possess a valid driver’s license. Frequent climbing of ladders, bending, kneeling, walking jobsites, and using hand tools and power tools.
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Event Marketing Coordinator
Odyssey Exposure INC. —Newark, OH
Managing the full lifecycle of each pop-up shift — setup, active fundraising, breakdown, and post-event reporting. We provide full paid training from day one.
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Clinical Research Coordinator- Greenback

Retina Sacramento MSO LLC
Sacramento, CA

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Job Details

Full-time
$31.00 - $44.50 an hour

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
On-the-job training
Dependent health insurance coverage
Vision insurance
Paid sick time

Qualifications

Phone communication
High school diploma or GED

Full Job Description

Come and join our team! We are a local growing private medical practice specializing in the diagnosis and treatment of patients with diseases of the retina and vitreous. We are looking for individuals who would like to establish a career in healthcare working with nationally recognized physicians. We provide on the job training giving you the ability to grow and advance your skills along with gaining innovative knowledge. Established in 1977, we have locations all over Northern California including Sacramento, Grass Valley, Roseville, Stockton, Modesto, Merced, Fairfield, Elk Grove, Folsom, Yuba City and Chico. Our physicians are nationally known, and we continue to be on the leading edge of retina care by utilizing the latest equipment and both participating in and designing new clinical trials to advance the state of care for retinal diseases. Join 250+ other team members working for our nationally recognized retina specialty practice in a fast paced, high volume medical office.

The research coordinator is primarily 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.

We seek a full-time clinical research coordinator to support our clinical research department. Although you must be able to work independently, you will be working directly with physicians, patients, research coordinators, clinical and business office staff and with pharmaceutical sponsor representatives to correctly and efficiently execute clinical research protocols. Collaboration and being a team player are essential to the success of this role.

As our clinical research coordinator, you will assist in the planning, development and implementation of clinical research trials involving the study of agents to treat diseases of the retina, macula and vitreous.

Responsibilities:

Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
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.)
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 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 to make any corrections needed to meet requirements and deadlines as needed
Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframe
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 the sponsor.

Strong communication skills
Retinal photography experience preferred

Minimum Requirements:

High School diploma or the equivalent
At least 2 years of clinical research experience or CRCC Certification/CCRP Certification

Physical Requirements:

Must be able to stand for long periods of time
Must be able to write
Must be able to hold arms at shoulder height
Must be able to communicate via telephone
Must have manual dexterity to work with ophthalmic equipment

Full-time immediate employee benefits:
Paid Time Off (PTO) 13 days per year, as accrued.
7 Paid Holidays per year.
Scrub Allowance
Ability to participate in company 401k plan offered through Fidelity.

On the first of the month following 30 days of employment benefits:
Medical insurance – employer pays 95% of premium of base HMO plan for employee (dependent coverage available for purchase).
Group dental, vision, life, and accident plans available for purchase.
Flexible Spending Account participation available.
Allows pre-tax deferrals of amounts for medical, dental or vision premiums
Allows pre-tax deferrals for dependent care expenses, subject to limitations

After 90 days of employment – Paid Sick Leave of 5 days per year.

After one year of service – 401K Plan Safe Harbor contribution (3% of annual earnings) received after plan year ends.

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Refine Your Search

training coordinator jobs in rocklin, ca

Clinical Research Coordinator- Greenback

Intake Coordinator Home Health

Patient Care Coordinator

Unit Secretary / Intake Coordinator

Coordinator, Training and Administration

Training Coordinator

Quality & Training Coordinator (Sacramento)

Sales and Marketing Coordinator

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