Top 24 Clinical research associate Jobs in Valencia, Ca

FSP Sr. CRA - Oncology Experience - US West
Thermo Fisher Scientific —California
- $72,000 - $145,000 a year
- Full-time
- RN License
- Writing skills
- English
- Commuter assistance
- Paid parental leave
9d
Clinical Research Associate
Advanced Bionics —Valencia, CA
- $79,000 - $99,000 a year
- Hybrid work
- Nursing
- Up to 50% travel
- English
- Paid parental leave
- Paid holidays
3d
Senior Clinical Research Associate
Advanced Bionics —Valencia, CA
- $100,000 - $125,000 a year
- Hybrid work
- Nursing
- Up to 50% travel
- 5 years
- Paid parental leave
- Paid holidays
3d
Senior Clinical Research Coordinator - Hematology/Oncology
UCLA Health —Westlake Village, CA
- $93,927.51 - $151,099.73 a year
- Mid-level
- Analysis skills
- Bachelor's degree
3d
Postdoctoral Researcher-Biomaterials and Hydrogel Engineering
TERASAKI INSITUTE FOR BIOMEDICAL INNOVATION —Woodland Hills, CA
- $70,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- Senior level
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA —Valencia, CA
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Postdoctoral Researcher-Biomaterials and Hydrogel Engineering
Terasaki Institute for Biomedical Innovation —Woodland Hills, CA
- $70,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- Senior level
Quick Apply
Regional Regulatory Specialist
Flourish Research —Northridge, CA
- $25 - $26 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator
ECN Operating LLC —Northridge, CA
- $17 - $19 an hour
- 8 hour shift
- Organizational skills
- Communication skills
- Entry level
Quick Apply
Medical Assistant - Clinical Research
CenExel Clinical Research —Sherman Oaks, CA
- $20.00 - $22.50 an hour
- Full-time
- Psychiatry
- Office
- Neurology
- Health savings account
- Health insurance
Quick Apply
5d
Clinical Research Assistant - Experienced Phlebotomist Required
Bayview Research Group, LLC —Valley Village, CA
- $25 an hour
- Part-time
- Anatomy knowledge
- Microsoft Excel
- Vital signs
- Health insurance
- Dental insurance
Quick Apply
5d
Clinical Data Manager - Data Integrity & Investigation
RDI —Van Nuys, CA
- $100,000 - $135,000 a year
- Full-time
- Senior level
- AD&D insurance
- Health insurance
Quick Apply
Clinical Research Coordinator II
Exer Medical Corporation —Sherman Oaks, CA
- $30 - $38 an hour
- Overtime
- Microsoft Word
- Spanish
- Microsoft Excel
Quick Apply
Postdoctoral Research Fellow Stem Cell Biology and Human iPSC Engineering
TERASAKI INSITUTE FOR BIOMEDICAL INNOVATION —Woodland Hills, CA
- $70,000 a year
- Full-time
- Doctor of Philosophy
- Senior level
- Communication skills
10d
Senior Field Clinical Engineer - NMPH - Remote within USA
Medtronic —Northridge, CA
- $108,000 - $162,000 a year
- Full-time
- Remote
- Clinic experience
- Clinic
- Driver's License
- Health savings account
- Employee stock purchase plan
Project Delivery Manager
IQVIA —Valencia, CA
- $80,200 - $167,200 a year
- Full-time
- Remote
- Computer literacy
- English
- Mid-level
- Work from home
Site Manager
ECN Operating LLC —Northridge, CA
- $80,000 a year
- Full-time
- Senior level
- Communication skills
Quick Apply
9d
Medical Assistant - Clinical Research
California Neuroscience Research, LLC —Sherman Oaks, CA
- $20.00 - $22.50 an hour
- Full-time
- Psychiatry
- Office
- Neurology
- Health insurance
- Dental insurance
Quick Apply
4d
Clinical Trial Supply & Logistics Coordinator
Andwin Scientific —Simi Valley, CA
- $52,000 - $72,000 a year
- Full-time
- ERP systems
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
4d

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FSP Sr. CRA - Oncology Experience - US West

Thermo Fisher Scientific -
California

Apply Now

Job Details

Full-time
$72,000 - $145,000 a year
9 days ago

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Customer communication
Driver's License

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
Valid driver's license where applicable
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers’ underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Working Conditions and Environment:
Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.
Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

Compensation and Benefits

The salary range estimated for this position based in California is $72,000.00–$145,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

Refine Your Search

clinical research associate jobs in valencia, ca

FSP Sr. CRA - Oncology Experience - US West

Clinical Research Associate

Senior Clinical Research Associate

Senior Clinical Research Coordinator - Hematology/Oncology

Postdoctoral Researcher-Biomaterials and Hydrogel Engineering

Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)

Postdoctoral Researcher-Biomaterials and Hydrogel Engineering

Regional Regulatory Specialist

Clinical Research Coordinator

Medical Assistant - Clinical Research

Clinical Research Assistant - Experienced Phlebotomist Required

Clinical Data Manager - Data Integrity & Investigation

Clinical Research Coordinator II

Postdoctoral Research Fellow Stem Cell Biology and Human iPSC Engineering

Senior Field Clinical Engineer - NMPH - Remote within USA

Project Delivery Manager

Site Manager

Medical Assistant - Clinical Research

Clinical Trial Supply & Logistics Coordinator

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