Clinical Research Associate I
$70k - $85kBiolinq Incorporated
Job Type Full-time Description WARNING about fake job posting scams. There has been a recent wave of scams whereby third parties post fake job openings using a bogus email address that resembles View email address on click.appcast.io . Under the guise of asking you to fill outan application, the scammers are attempting to gather your personal information. See the Federal Trade Commission's warning on this topic at: The only official source for actual Biolinq job postings/openings is at . While other job sites (such as LinkedIn, Indeed or Glassdoor) may pull from Biolinq's careers web page, you should visit to verify the accuracy of the openings found on third party web sites. About the Company Biolinq is a venture-backed digital health company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes. This dynamic role is a part of a team of engineers and scientists developing a novel intradermal biosensor technology and the associated software data extraction and rendering SDK that will transform the way people manage their metabolic health. Job Purpose To support and contribute to the Clinical Affairs team execution and conduct of Biolinq sponsored clinical studies. Able to work under direct supervision of the Manager of Clinical Operations as well as collaboratively with other departments. Responsible for assigned tasks to support study planning and ensuring requirements are appropriately executed to meet deadlines, quality expectations, and priorities. A FCRA is expected to foster and maintain a good working relationship with clinical sites including addressing and resolving issues while ensuring their compliance with the study protocol and regulatory requirements. Duties and Responsibilities Serves as a team member in all aspects of clinical study execution Provide clinical support with application and removal of a novel wearable biosensor device Act as a research coordinator or monitor for in-house studies and external studies including subject recruitment and follow-ups Maintain organization, timely ordering and shipping of supplies and equipment required for clinical studies Assist with the quality control of study-related documents and devices and be accountable for their correct distribution Assist with developing clinical study materials under direct supervision Coordinate study-related meetings and provide training to study staff and subjects at clinical sites Provide support to management for preparing documentation, reports, and presentations Conduct monitoring visits for Biolinq sponsored studies including completion of monitoring report and oversee any action items to completion Assist with distribution of regulatory documents and the maintenance of trial master files Assist with departmental audits of clinical studies and procedures Perform scribe function during clinical meetings and produce meeting minutes for management review Collaborate effectively with peers and leadership across departments Travel required up to 70% Other duties as assigned Requirements Qualifications Bachelor's (BA or BS) degree in a STEM discipline, and 2-5 years of related experience or Master's degree in a STEM discipline and 0-3 years of related experience Familiar with Good Clinical Practice guidelines and regulations for conducting human clinical studies Knowledge of the Health Insurance Portability and Accountability Act (HIPAA) and the ability to manage Protected Health Information (PHI) Complete tasks under minimal supervision Works on moderately complex problems where analysis of situations or data requires evaluation Exercises judgment within defined procedures and practices to determine appropriate action Demonstrates technical proficiency Personal computer skills, including proficiency in word processing, spreadsheet, and electronic databases Must maintain good communication skills with patients and health care professionals Ability to engage in continuous learning and self-development Working Conditions Position will be based at Biolinq Headquarters (non-remote) General office, Physician offices, Medical Clinics, Hospitals, and Laboratory Travel required up to 70% and will be based on number of clinical studies being conducted Hours of work may be outside of the traditional M-F work week Physical Requirements While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office environment. Employee may occasionally lift/or move up to 15 pounds. BENEFITS Medical, dental, vision, health savings account, flexible spending account, life and long-term disability insurance, 401(k) plan, holidays, and PTO. At Biolinq we fully subscribe to the principles of Equal Employment Opportunity. It is our policy to provide employment, compensation, and other benefits related to employment based on qualifications, without regard to race, color, religion, national origin, age, sex, veteran status, genetic information, disability, or any other basis prohibited by federal, state or local law. In accordance with requirements of the Americans with Disabilities Act and applicable federal, state and/or local laws, it is our policy to provide reasonable accommodation upon request during the application process to applicants in order that they may be given a full and fair opportunity to be considered for employment. As an Equal Opportunity Employer, we intend to comply fully with applicable federal, state and/or local employment laws and the information requested on this application will only be used for purposes consistent with those laws. To the extent required by applicable law, The Company maintains a smoke- free workplace. As part of our efforts to ensure fair and equal pay based on merit, Biolinq supports pay transparency internally and during the recruitment process. The U.S. base salary range reasonably expected to be paid for this role is: $70,000 to $85,000 per year. We may ultimately pay more or less than the posted range. Actual compensation packages are commensurate with experience and based on a variety of factors that are unique to each candidate including, but not limited to: skill set, depth of experience, education, certifications, and specific work location. The range displayed reflects the minimum and maximum target for new hire salaries for the job across the U.S. The total compensation package for this position may also include an annual performance bonus and/or other applicable incentive compensation plans. Biolinq also offers a comprehensive package of benefits including paid time off (vacation, holidays, sick time, parental leave), medical/dental/vision insurance, and 401(k) to eligible employees, subject to the terms and conditions of the applicable plans and any written agreement between the parties. Your recruiter can share more about the total compensation package during the hiring process. Please note: The information contained herein is not intended to be an all-inclusive list of duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Biolinq Talent Acquisition at View email address on click.appcast.io Salary Description $70,000-$85,000 per year
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated El Cajon, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring visits (selection...SuggestedFull timePart timeLocal areaImmediate start$36.36 - $50.9 per hour
## Clinical Research AssociateApplylocations: San Diego, CAtime type: Full timeposted on: Posted Todayjob requisition id: REQ20176956The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute...SuggestedHourly payWork experience placementLocal areaRemote work$65 - $90 per hour
...C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the San Diego region. This opportunity is ideal for professionals who enjoy working closely with investigative sites while maintaining strong oversight of complex...SuggestedHourly payContract workFor contractorsRemote work$95k - $124k
...Department: 106600 Clinical Operations | Location: San Diego Position Summary This role reports to the Associate Director, Clinical Operations and involves coordinating, tracking, and managing daily oversight of multiple clinical studies. The candidate will support internal...SuggestedTemporary workWork at officeRemote work- ...activated at the tumor site. Our first clinical product received marketing approval in Japan... ...training activities for clinical research teams and site staff. Site Contracts and... ...vendor and site contract terms and verify associated invoices for accuracy and compliance with...SuggestedFull timeContract workWork at officeFlexible hours
- The University of Southern California is seeking a Clinical Research Associate in San Diego, California. This role involves oversight of clinical trials, ensuring adherence to regulatory guidelines and evaluating data integrity. Candidates should have a Bachelor’s degree...
$59.91k - $71.45k
The University of California San Diego is hiring a Research Associate for the Shiley-Marcos Alzheimer's Disease Research Center. The role involves participant recruitment, administration of cognitive assessments, and data management. Qualifications include a Bachelor’s...$42.02 - $57.51 per hour
Overview The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an... ...new treatments for Alzheimer’s Disease (AD) through innovative clinical trials. Responsibilities Conduct onsite and remote monitoring...Hourly payLocal areaRemote work- Clinical Resource Network (CRN) in San Diego is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This position focuses on in-house clinical operations with minimal travel requirements. The ideal candidate will have at...Contract workWork at office
$60 - $75 per hour
A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This is an in‑house clinical operations role (not a field monitoring position) with minimal travel...Hourly payLong term contractFull timeContract workWork at officeRemote work- ...services in our Allergan Aesthetics portfolio. Job Description Purpose: 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...Contract workTemporary workLocal area
$70k - $85k
Biolinq is looking for a clinical professional to support its Clinical Affairs team with the execution of sponsored studies in San Diego, California. The candidate must possess a bachelor's degree in a STEM discipline and have 2-5 years of related experience or a master...$28.69 per hour
UC San Diego is seeking a Staff Research Associate through its Temporary Employment Services. This role involves assisting with research protocols... ...relevant academic qualifications and experience conducting clinical research. Compensation is $28.69/hr, with a duration of...Temporary work$42.02 - $57.51 per hour
Itlearn360 is seeking a Clinical Monitor to ensure compliance and safety in clinical trials. Responsibilities include conducting monitoring visits and reviewing study data. The ideal candidate has a Bachelor's degree, at least 2 years of relevant experience, and a thorough...Hourly pay$99.1k - $141.89k
...The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute... ...new treatments for Alzheimer’s Disease (AD) through innovative clinical trials. Incumbent will support the medical monitoring team in...- Headlands Research is seeking Clinical Research Assistants to support the execution of clinical trials across multiple locations. This position is ideal for individuals with laboratory or research experience who wish to transition into clinical roles. Responsibilities...
- Clinical Research Assistant Opportunities - Multiple Locations Nationwide At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting‑edge technology and...
- UC San Diego is looking for a Clinical Research Coordinator Assistant to oversee and manage a clinical trial related to substance use disorders. The role includes responsibilities such as participant recruitment, data collection, and working closely with study clinicians...
- ...University of California - San Diego Medical Centers is looking for an Assistant to support clinical trials in cardiology. You will work closely with coordinators and the research team, conducting patient screenings and managing lab supplies. This role requires a high...Flexible hours
$54.77k - $64.58k
The University of California San Diego is seeking a Clinical Trials Research Assistant in San Diego. This role involves assisting the research team with communication between sponsors and conducting patient screenings, interviews, and data collection. You will also handle...Flexible hours- ...staff). In addition, the Department has 57 clinical residents and fellows distributed across the Divisions. The missions of research, education and patient care are... ...QUALIFICATIONS Certification as a Clinical Research Associate or Coordinator. Experience working with research...
$77.09k - $100k
...Job Description Sanford Burnham Prebys is much more than a research facility and hub for innovation; it’s a vibrant global community... ...wellness programs and events throughout the year such as flu shot clinics, health fairs, lunch-and-learns, yoga classes, and more!...Local areaRemote workWork from homeWorldwideHome office- ...to provide departmental administrative support in the area of Clinical Affairs, including: Perform quality checks, uploads and tracking... ...and tracking of clinical study supplies to Contract Research Organizations (CROs) and clinical centers (e.g. study binders,...Contract work
$54.77k - $64.58k
DESCRIPTION The incumbent will serve as an assistant to the clinical trials research coordinators, director of cardiovascular research and Principal Investigators in cardiology. The incumbent will perform standard repetitive field procedures that require technical, scientific...Hourly payFlexible hours$26 - $31 per hour
...Maintain a safe work environment and wear appropriate personal protective equipment Minimum Qualification Associate’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology California state issued Medical Lab Technician license (MLT)...Hourly payFlexible hoursShift work$66.75k - $107.41k
Clinical Research Coordinator Assistant job at UC San Diego. San Diego, CA. Filing Deadline: Wed 8/13/2025 UC San Diego values equity, diversity... ...QUALIFICATIONS Certification as a Clinical Research Associate or Coordinator or as a Certified Phlebotomist. Licensed by...Hourly payLocal areaAfternoon shift$84.06k - $88.74k
...Total Openings 1 Work Schedule Days, 8 hrs/day, Mon-Fri #138411 Research Administrator 3 Extended Deadline Thu 6/18/2026 Apply Now UC... ...federal, state, local and private sponsors. Involves activities associated with forecasting, planning, and managing of research...Hourly payContract workLocal areaWorldwideAfternoon shift$75k - $93.4k
...Research Administrator 3 (#139876) Filing Deadline: Fri 6/12/2026 Payroll Title: RSCH ADM 3 Department: ORU CORE SERVICES UNIT Hiring... ...federal, state, local and private sponsors. Involves activities associated with forecasting, planning, and managing of research...Hourly payContract workSummer workLocal areaFlexible hours$75.15k - $109.45k
...position at the intermediate, fully operational level of the Research Administrator series. The incumbent applies acquired job skills... ...federal, state, local and private sponsors. Involves activities associated with forecasting, planning, and managing of research...Hourly payContract workSummer workLocal areaWeekend work$18.67 - $24 per hour
About Us Scripps Research is a nonprofit biomedical institute ranked as one of the most influential in the world for its impact on innovation. We celebrated our 100‑year legacy in 2024. This significant milestone marks a century of seminal discoveries in immunology, infectious...Hourly payTraineeshipFlexible hours
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