CrawlJobs Logo

Staff Research Associate

ucsd.edu Logo

UC San Diego

Location Icon

Location:
United States , La Jolla

Category Icon
Category:
IT - Administration

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

59905.00 - 71451.00 USD / Year ▼
Save Job
Save Icon
Apply Position

Job Description:

Under close technical supervision the incumbent will assist the Principal Investigator in research on the development and evolution of morphology of the musculoskeletal system primarily using rodents as the research models. Incumbent will assist in research by performing a wide variety of standard molecular biology techniques (PCR, gel electrophoresis, DNA transformation), tissue histology (fixation, sample preparation, and sectioning), cell and tissue culture, and animal husbandry. They will also assist the PI by performing the following duties: order and maintain lab equipment and supplies, maintain cleanliness and safety of lab, prepare buffers and solutions, and perform other general lab duties. Perform other duties as assigned.

Job Responsibility:

  • Assist the Principal Investigator in research on the development and evolution of morphology of the musculoskeletal system primarily using rodents as the research models
  • Assist in research by performing a wide variety of standard molecular biology techniques (PCR, gel electrophoresis, DNA transformation), tissue histology (fixation, sample preparation, and sectioning), cell and tissue culture, and animal husbandry
  • Assist the PI by performing the following duties: order and maintain lab equipment and supplies, maintain cleanliness and safety of lab, prepare buffers and solutions, and perform other general lab duties
  • Perform other duties as assigned

Requirements:

  • Theoretical and practical knowledge of molecular, cell, and developmental biology gained through a Bachelor's degree in Biology or a related field and/or equivalent combination of education and experience
  • Demonstrated experience performing standard and repetitive molecular biology techniques such as RNA and DNA preparation, molecular cloning, gel electrophoresis, PCR, etc.
  • Experience with histology and immunostaining procedures
  • Experience with sterile techniques, calculating molarity and dilutions, and preparing buffers, solutions and growth media
  • Experience operating laboratory equipment, including centrifuges, ultracentrifuges, balances, pH meters
  • Demonstrated knowledge of principles of basic light microscopy
  • experience with compound microscopes
  • Knowledge of specialized scientific terminology
  • Ability to learn new experimental methods as required
  • Ability to work independently or collaboratively on a research project
  • Ability to record scientific data in a well-organized laboratory notebook
  • Good organizational skills including ability to keep clear and accurate records
  • Knowledge of purchasing and reimbursement procedures
  • Skills in maintaining steady levels of lab supplies, maintaining purchasing records, and training others in purchasing procedures
  • Effective (English) oral and written communication skills
  • Also good interpersonal communication skills including tact, diplomacy, and flexibility with students, staff, faculty, and visitors of various cultures and backgrounds
  • Experience using MAC or PC, and associated software including FilemakerPro, MS Word, and Excel
  • Knowledge/understanding and at least some experience with Safety Data Sheets, hazard communication and Injury and Illness Prevention Program
  • Familiarity with a Chemical Hygiene Plan addressing safety precautions including appropriate clothing and shoes, safe handling of chemicals, use of protective items
  • Willingness and ability to keep safety training current and consistent with research involvement
  • Ability to confidently direct others in safety regulations to maintain a safe and efficiently functioning lab environment
  • Knowledge of humane methods of caring for lab animals, such as mice or rats
  • Sensitivity to the needs of caged laboratory animals in compliance with AAALAC standards
  • Willingness and demonstrated ability to embrace and consistently uphold the principles of community for a collaborative work environment

Additional Information:

Job Posted:
May 17, 2026

Expiration:
May 28, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
UC San Diego - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon
PREMIUM
More languages and countries
Unlock 29494 hidden job offers
Languages
English Čeština Deutsch Ελληνικά Español Français +15
Countries
United States United Kingdom India Canada Australia +
See plans
Plans from $2.99 / month

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Staff Research Associate

Clinical Research Associate II/Sr. Clinical Research Associate - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Ability to travel 60-80%
  • Valid driver’s license and passport required
  • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Job Responsibility
Job Responsibility
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • Serve as the primary point of contact for assigned investigator sites
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • Provide protocol training to, and address protocol related questions from the investigator site staff when required
  • Attend investigator meeting when required (virtual or F2F)
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
China , Chengdu
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Research Associate II

Clinical Research Associate - Remote - FSP. ICON plc is a world-leading healthca...
Location
Location
Greece , Athens
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Research Associate

Proclinical is seeking two Clinical Research Associates to join our client on a ...
Location
Location
United Kingdom , City of London
Salary
Salary:
Not provided
proclinical.com Logo
Proclinical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in Clinical research, preferably within a CRO or pharmaceutical setting
  • Previous history of independent monitoring experience is required
  • Background in diabetes or obesity therapeutic areas is beneficial but not essential
  • Strong organizational and communication skills
  • Capacity to travel regionally as the business requires
  • Academic candidates with relevant experience, including monitoring, will also be considered
Job Responsibility
Job Responsibility
  • Conduct site visits within the select region
  • Perform monitoring activities to ensure adherence to compliance standards with study protocols, regulatory requirements, and GCP
  • Work closely with site staff to ensure proper documentation and data collection
  • Support study start-up, maintenance, and close-out activities
  • Maintain effective communication with study teams and stakeholders
  • Provide updates and reports on site performance and study progress
  • Fulltime
Read More
Arrow Right

Clinical Research Associate

The Clinical Research Associate (Monitor) is responsible for supporting clinical...
Location
Location
Salary
Salary:
Not provided
honorvettech.com Logo
HonorVet Technologies
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. or B.A. and/or an equivalent combination of education or experience
  • Minimum of 3 years of experience directly related to the execution of clinical research studies
  • Available to travel (up to 60%) on short notice and independently manage travel schedules
  • Must have analytical skills, be detail oriented and have good interpersonal skills
  • Knowledge of agency guidelines and requirements
  • Effective written and verbal communication skills
  • Ability to communicate at all levels of an organization
  • PC skills
  • word processing, spreadsheet, database, Internet search and utilization
  • Flexible and able to work in a fast-paced environment
Job Responsibility
Job Responsibility
  • Collaborate with team members in the evaluation and establishment of clinical study sites by performing site qualification visits and site initiation visits to ensure applicability of sites for planned study according to application regulatory requirements
  • Collaborate with Senior Clinical Research Associate to create source documentation/CRFs in alignment with protocol requirements
  • Collaborate with sites and internal stakeholders to align and implement site specific language for each consent/assent and support Institutional Review Board (IRB) submissions
  • Train site staff on protocol requirements, source documentation, and case report form completion
  • Conduct regular monitoring visits to ensure study protocol compliance, primary data collection is recorded properly, and appropriate reporting is being conducted
  • Conduct clinical study site close-out visits and ensure site files are complete, accurate and up to date
  • File site related documents real-time to ensure Trial Master Files are complete and accurate at all times
  • Provide study specific information and support report validation activities as requested for clinical study reports
  • Participates in team meetings and document meeting minutes and tracks action items
  • Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent attention to detail
  • Good written and verbal communication skills
  • Good collaboration and interpersonal skills
  • Good negotiation skills
  • Proficient in written and spoken English language required
  • Fluency in local language(s) required
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
  • Good knowledge of relevant local regulations
  • Good medical knowledge and ability to learn relevant Client Therapeutic Areas
  • Basic understanding of the drug development process
Job Responsibility
Job Responsibility
  • Contributes to the selection of potential investigators
  • In some countries, as required, accountable for study start-up and regulatory maintenance
  • Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles
  • Confirms that site staff have completed and documented the required training appropriately
  • Actively participates in Local Study Team (LST) meetings
  • Contributes to National Investigators meetings, as applicable
  • Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
  • Shares information on patient recruitment and study site progress
  • Drives performance at the sites
  • Proactively identifies and ensures timely resolution to study-related issues
What we offer
What we offer
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
South Korea , Seoul
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • Excellent written and verbal communication in English
  • Good social skills enabling you to deal with queries in a timely manner
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
  • Must have oncology studies experience
  • At least 1.5 yrs SIT-On Site Monitoring Experience
Job Responsibility
Job Responsibility
  • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
  • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
  • you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right