Top 115 Clinical trial associate Jobs in San Diego Ca

Clinical Research Associate II - Southern CA
AbbVie —San Diego, CA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Bachelor's degree
- Paid holidays
- Health insurance
5d
Clinical Research Associate (CRA)
ResMed —San Diego, CA
- $86,000 - $128,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Commuter assistance
- Health savings account
19h
Specialist, Clinical Trials
Neurocrine Bioscience —San Diego, CA
- $89,800 - $123,000 a year
- Full-time
- Psychiatry
- Computer literacy
- Bachelor of Science
- Paid holidays
- Health insurance
7d
Clinical Research Coordinator I
CAMRIS International, LLC —San Diego, CA
- $70,304 - $73,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Mid-level
- Health savings account
- AD&D insurance
Clinical Research Coordinator (Non-RN) - Research & Clinical Management
Rady Children's Health —San Diego, CA
- $34.14 - $46.94 an hour
- Vital signs
- Management
- Word processing
3d
Clinical Data Associate II
Viking Therapeutics, Inc. —San Diego, CA
- $75,000 - $90,000 a year
- Writing skills
- System design
- Mid-level
Quick Apply
Clinical Research Coordinator
Medical Research Team- San Diego —San Diego, CA
- $30 - $75 an hour
- Part-time
- Hybrid work
- Mid-level
- Analysis skills
- Supervising experience
- Tuition reimbursement
- Professional development assistance
Quick Apply
Research Associate - Cancer Center
UC San Diego Health —San Diego, CA
- $32.79 - $52.75 an hour
- 8 hour shift
- Pass drug screening
- Mid-level
- Math
12d
Clinical Trial Manager/Senior Clinical Trial Manager
Janux Therapeutics —San Diego, CA
- $140,000 - $178,000 a year
- Full-time
- Hybrid work
- Office
- 8 years
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
10d
Staff Research Associate I - Pediatrics
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Computer literacy
- Pass drug screening
- Criminal background check
8d
Senior Clinical Trial Manager, Clinical Operations
Iambic Therapeutics, Inc —San Diego, CA
- $152,000 - $190,000 a year
- Full-time
- 7 years
- Bachelor's degree
- Travel
- Flexible spending account
- 401(k) matching
Assistant Clinical Research Coordinator
CAMRIS International, LLC —San Diego, CA
- $56,226.40 - $62,144.97 a year
- Full-time
- Mid-level
- Organizational skills
- Communication skills
- Health savings account
- AD&D insurance
Clinical Research Coordinator
Odyssey Consulting —Naval Medical Center San Diego, CA
- $80,000 - $90,793 a year
- Weekends as needed
- Hybrid work
- Mid-level
- Office
- 3 years
- Health savings account
- Paid holidays
Associate Clinical Project Manager / Clinical Project Manager
n-Lorem —San Diego, CA
- $80,000 - $100,000 a year
- Full-time
- Hybrid work
- Customer service
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
10d
Clinical Research Coordinator
Medical Oncology Associates of San Diego —San Diego, CA
- $70,000 - $80,000 a year
- 8 hour shift
- Patient monitoring
- Bachelor of Science
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Manager, Clinical Operations (on-site)
Neomorph, Inc. —San Diego, CA
- $147,000 - $168,000 a year
- Hybrid work
- 5 years
- Bachelor's degree
- Continuous improvement
- Paid parental leave
- Health savings account
7d
Associate Director, Clinical Operations
Travere Therapeutics —San Diego, CA
- $150,000 - $195,000 a year
- Online Application
- Nursing
- Microsoft Office
- 8 years
- Health insurance
- Paid time off
Clinical Research Coordinator
No-Resistance Consulting Group —San Diego, CA
- $22.50 - $25.00 an hour
- Full-time
- Urgent Care
- Clinic
- In-person
- Health insurance
- Dental insurance
Quick Apply
9d
Sr. Clinical Trial Manager
Janux Therapeutics —San Diego, CA
- $165,000 - $180,000 a year
- Full-time
- Hybrid work
- Travel
- US work authorization
- Contracts
- Health savings account
- Employee stock purchase plan
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —San Diego, CA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply

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Clinical Research Associate II - Southern CA

AbbVie -
San Diego, CA

Apply Now

Job Details

Full-time
$84,500 - $162,000 a year
5 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

ICH guidelines
Bachelor's degree
Research regulatory compliance
Cross-functional collaboration
Pharmaceutical research experience
Stakeholder relationship building

Full Job Description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

This positions is field based / remote in Southern CA. Candidates must reside in Southern California and be willing to travel for site visits.

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.

Responsibilities

Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning.
Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.
Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.
Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies). Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.
Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
May participate in global/local task forces and initiatives. Responsible for activities as assigned by manager.
Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.
Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution. Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach.
Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
Ensures audit and regulatory inspection readiness at assigned clinical site at all times.
Manages investigator payments as per executed contract obligations, as applicable.

Qualifications

Education: Bachelor’s degree or equivalent degree; health related preferred (e.g. Medical, Scientific, Nursing, Pharmacy).
Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials. Familiar with risk‐based monitoring approach, onsite and offsite monitoring.
Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.
Demonstrate strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
Advanced ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.
Strong interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.
Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues.
Acts with integrity in accordance with AbbVie code of business conduct and leadership values. Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role atthe time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors includinggeographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested,and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to aparticular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion,consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Apply Now

Refine Your Search

clinical trial associate jobs in san diego ca

Clinical Research Associate II - Southern CA

Clinical Research Associate (CRA)

Specialist, Clinical Trials

Clinical Research Coordinator I

Clinical Research Coordinator (Non-RN) - Research & Clinical Management

Clinical Data Associate II

Clinical Research Coordinator

Research Associate - Cancer Center

Clinical Trial Manager/Senior Clinical Trial Manager

Staff Research Associate I - Pediatrics

Senior Clinical Trial Manager, Clinical Operations

Assistant Clinical Research Coordinator

Clinical Research Coordinator

Associate Clinical Project Manager / Clinical Project Manager

Clinical Research Coordinator

Clinical Trial Manager, Clinical Operations (on-site)

Associate Director, Clinical Operations

Clinical Research Coordinator

Sr. Clinical Trial Manager

Senior Clinical Research Associate (level dependent on experience)

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