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Initiation Clinical Research Associate Ii Jobs in San Diego, California

Research Associate Ii / Lvn, San Diego Clinical Trials (Durational W/Benefits)
By Kaiser Permanente At , San Diego $63,500 - $82,060 a year
Must be able to work in a Labor/Management Partnership environment.
Adheres to compliance and privacy/ confidentiality requirements and standards. Adheres to GCP and compliance regulations for clinical trials.
Acquires and maintains knowledge of KP systems and databases.
Minimum one (1) year of experience coordinating research projects under specific guidance.
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; OR
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR
Research Associate Ii Jobs
By DermTech At San Diego, CA, United States
Manage sample processing for internal experiments, collaborations, and client clinical trials.
BA/BS and 3- 5 years or MS and 0-2 years of industry experience in molecular biology, microbiology, genomics, or related discipline.
Good knowledge of the use of clinical data sets and public databases.
Creative mindset with strong decision-making and troubleshooting skills.
Desire and ability to learn new skills and a willingness to undertake training courses for continued professional development.
Collaborative attitude with the ability to communicate with individuals across the spectrum of scientific knowledge.
Research Associate I/Ii
By Capricor Therapeutics, Inc. At San Diego, CA, United States
Bachelor’s degree required; preferably in the biological sciences (or experience in biology research)
2+ years of sterile tissue culture experience preferred
CGMP experience preferred but not required
Cell culture and molecular biology skills are required
Experience with flow cytometry, functional assays, DNA, RNA and protein analysis is preferred
Previous experience with handling small animals (e.g. rodents) is preferred
Clinical Research Associate Ii
By DermTech At San Diego Metropolitan Area, United States
Effective time and financial management skills.
Or equivalent combination of education and experience
or equivalent combination of education and experience
Years of independent monitoring experience within a Contract Research Organization/Pharmaceutical company
Good therapeutic and protocol knowledge as provided in-company training.
Strong written and verbal communication skills including good command of the English language.
Research Associate Ii / Senior Research Associate Ii, Cell Culturing - Simply Biotech
By TalentZök At Carlsbad, CA, United States
Bachelor's degree with 3+ years of industry experience
Must have experience with mammalian cell culturing experience
Experience with cell transfection is a big plus
Some molecular biology knowledge is a plus
Research Associate Ii Jobs
By DermTech At San Diego Metropolitan Area, United States
Liaise with the Research and Development team to communicate Clinical Operations Laboratory requirements during the assay development process.
Manage samples from experiments, collaborations, and clinical trials.
Basic knowledge of CLIA, CAP, and/or FDA regulations and Quality Systems.
Good knowledge in the use of clinical data sets and public databases.
Creative mindset with strong decision-making and troubleshooting skills.
Desire and ability to learn new skills and a willingness to undertake training courses for continued professional development.
Research Associate Ii - Exploratory R&D
By BioLegend At San Diego, CA, United States
Minimum Qualifications – Education And Experience
Preferred Qualifications – Education And Experience
Other projects or responsibilities as may be required.
At least 2 years of relevant experience working in an academic or industry laboratory
0-1 years of experience with SDS-PAGE, ELISA, and flow cytometry.
Highly experienced in mammalian cell culture
Research Associate Ii Jobs
By Hydrogen Group At Oceanside, CA, United States
Demonstrates ability to recognize anomalous and inconsistent results and interpret experimental outcomes.
Hands-on execution of all aspects of purification process development, process scale up and GMP manufacturing support.
Ability to work with increasing independence in the initiation and execution of laboratory experimentation.
Willingness to proactively seeking out senior personnel to define goals, design experiments, discuss results and suggest next steps.
*Please apply with your up to date CV to be considered for this role*
Essential Duties and Job Functions:
Clinical Research Associate Ii
By Labcorp At , San Diego, 92128, Ca $90,000 - $125,000 a year
Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process
Good planning, organization and problem-solving abilities; Ability to work with minimal supervision
Organize and make presentations at Investigator Meetings
Participate in the development of protocols and Case Report Forms as assigned
Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
Research Assistant Ii Jobs
By San Diego State University Research Foundation At , San Diego, 92120, Ca
OR - Equivalent of one year related experience in lieu of coursework
Completion of sufficient lower division coursework
San Diego State University Research Foundation is an EEO/AA/Disability/Vets Employer
in Translational Emotion Neuroscience and Development Lab
a full-time post-baccalaureate research assistant
Research Associate Ii Jobs
By Cytokinetics At South San Francisco, CA, United States
Help maintain research lab productivity by adhering to outlined group responsibilities and safety procedures.
Organized, attention to detail, excellent record-keeping skills, excellent verbal and written communication skills.
Display communication skills that will allow you to collaborate with both team members and partners outside the group.
Provide support, guidance, and mentorship for experiment design, data analysis, and result communication back to the team
Contribute to exploratory research and lead optimization projects, and collaborate closely with colleagues in other groups
Summarize/interpret data and present findings in research meetings
Research Associate Ii Jobs
By Nautilus Biotechnology At San Carlos, CA, United States
1 year work experience with proteins or cell lines is necessary
Experience with high-throughout ELISA's is highly preferred
Experience with performing assays on automated liquid handlers a plus
A minimum of 1 year of experience measuring probe-protein interactions with ELISA or similar techniques
Phage display experience is preferred
Highly organized with experience in maintaining large reagent catalogues
Research Associate Ii/Sra - Mammalian Cell Translation
By Metagenomi At Emeryville, CA, United States
Demonstrated scientific skills and knowledge of cloning, gene editing technologies, pooled and/or arrayed cell-based screening
Experience with mammalian cell culture and flow cytometry or microscopy
Effective oral and written communication, prioritization and organizational skills
Optimize and execute high-throughput pooled screens to determine strategies to improve performance of editing systems
Contribute to the design custom assays to assess impact of novel gene editing tools
Work cross-functionally across Metagenomi to move findings forward
Research Associate Ii, Vector Biosciences
By Astellas Gene Therapies At South San Francisco, CA, United States
Participate in sample management activities such as receiving, processing, storage, and shipping pre-clinical samples
Collaborate in laboratory management activities such as receiving, tracking, storage, and maintenance of laboratory reagent stock
Demonstrated experience with routine molecular biology techniques (DNA/RNA/protein isolation, cDNA synthesis, RT-PCR, qPCR, digital PCR, western blot, and immunofluorescence)
Strong written and verbal communication skills
Experience working with viruses, especially Adeno-Associated Virus (AAV)
Be BOLD (Find a Way)
Research Associate Ii / Sr. Research Associate
By Initial Therapeutics At South San Francisco, CA, United States
Experience with conducting low to medium throughput cell-based and biochemical screens using a variety of assay technologies.
Experience with designing and developing cell-based and biochemical assays to support lead optimization and/or mechanism of action studies.
Experience with High Content Imaging would be a plus.
Excellent communication (oral and written) and interpersonal skills.
If you want to stand out, please provide a cover letter hi-lighting your relevant qualifications.
Ability to work in an interdisciplinary, dynamic work environment.
Research Associate Ii, Vector Biosciences
By Astellas At , South San Francisco, 94080, Ca $72,800 - $97,000 a year
Experience with AKTA FPLC for AAV purification.
Purification and characterization of AAV vectors using column chromatography.
Analysis of purified AAV vectors by SDS-PAGE, agarose gel electrophoresis, ddPCR, RT-PCR and UV.
Support AAV production by maintaining, banking, and transfecting mammalian cells in culture.
Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to produce novel AAV vectors.
Medical, Dental and Vision Insurance
Research Associate Ii - Translational Neuroscience
By Inscopix, Inc. At Mountain View, CA, United States
Manage animal colonies and necessary equipment/supplies to perform research studies
BS or MS in Neuroscience or in a related field, with at least 2 years of lab-based experience
Excellent surgical skills, including evidence of precise stereotaxic technique
Extensive experience with rodent handling and behavioral assays
Experience maintaining inventory and ordering lab supplies
Perform data processing and documentation of all experimental results
Clinical Research Coordinator Ii
By CEDARS-SINAI At , Los Angeles, Ca $28.30 - $48.11 an hour
Job Summary: Key Job Responsibilities:
2 years Clinical research related experience
Establishes effective working relationships with cross-functional team(s)
Clinical Research Associate Ii/Certified Phlebotomy Technician (Cpt) - Cancer Biobank
By CEDARS-SINAI At , Los Angeles, Ca $21.26 - $36.14 an hour
Participates in required training and education programs. May be involved in training and education of other Clinical Research Associates.
1 year-Clinical Research Related Experience
SOCRA or ACRP certification, preferred
Works with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Completes Case Report Forms (CRFs).
Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Coordinator I/Ii
By Fred Hutch At Seattle, WA, United States
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.
Research Associate I/Ii
By Commonwealth Sciences, Inc. At Greater Boston, United States
Must have 1-3 years experience with molecular and in vivo techniques.
Must have experience with mouse colony maintenance.
Responsibilities of the Research Associate I/II:
Requirements of the Research Associate I/II:
Will perform and/or coordinate a wide range of highly sophisticated laboratory techniques to analyze the functions of immunoregulatory pathways.
Responsible for T cell function, cytokine ELISA assays, and multiparameter flow cytometry).
Clinical Research Assistant Ii - Leukemia Research In Ccto
By Beth Israel Deaconess Medical Center At , Boston
1-3 years of related work experience in a medical setting and/or in clinical research required.
Working knowledge of computerized data required including word processing, spreadsheets and databases.
Independence of Action: Ability to follow general instructions and procedures as provided. Work is monitored by supervisor/manager.
Checks all eligibility and ineligibility criteria with patients' medical record. Verifies information with clinical research nurse and/or principal investigator.
Bachelor's degree required; Master's degree preferred.
Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
Clinical Research Associate Ii
By BeiGene At , Remote $90,500 - $120,500 a year
Familiar with industry CTMS and data management systems
Provides site level management for established protocols and portfolio under general supervision
Project Management - Communicates changes and progress; Completes projects on time and budget.
Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
Excellent communication and interpersonal skills
Clinical Research Coordinator Ii
By Sutter Health At , Palo Alto $40.85 - $61.28 an hour
Mentors and fosters a constructive teaching environment that helps students and new teammates build confidence in their skills, knowledge and abilities.
Performs information management functions, including maintaining databases, entering and auditing data, may perform trending.
Ensures compliance with protocol guidelines and requirements of regulatory agencies.
2 years experience conducting clinical research.
2 years experience ensuring compliance with research regulations.
Equivalent experience will be accepted in lieu of the required degree or diploma.
Clinical Research Coordinator Ii
By University of Alabama at Birmingham At , Birmingham

Work Arrangement (final schedule to be determined by the department/hiring manager): Remote/Hybrid Eligible

This position will be responsible for research activities and research documentation processes.

Clinical Research Associate Ii - Phoenix / Tucson
By ICON At , Phoenix
Knowledge of ICH and local regulatory authority regulations regarding drug
Experience in monitoring all trial components (PSSV to COV)
Ability to travel as needed (greater than 40%)
Clinical Research Coordinator Ii
By Legacy Health At , Portland, 97210
Proficient in word processing, spreadsheet management and database management.
Bachelor’s degree in a related field or equivalent healthcare experience.
One year of experience in clinical research coordination.
Excellent interpersonal skills, with proven written and verbal competencies.
Specialized knowledge of the research process and federal regulations.
Good analytical and problem-solving skills.
Clinical Research Associate Ii (Cra Ii)- Ophthalmology (Central)
By Parexel At , Remote
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

Are you looking for an exciting opportunity to join a dynamic team of Clinical Research Associates and help shape the future of medical research? We are looking for a Clinical Research Associate II to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate II, you will be responsible for the initiation, monitoring, and close-out of clinical trials. You will also be responsible for ensuring compliance with applicable regulations and guidelines. If you are a motivated individual with a passion for clinical research, this may be the perfect opportunity for you!

Overview The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This role requires a high level of knowledge and experience in clinical research and the ability to effectively manage multiple projects. Detailed Job Description The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This includes developing and executing study protocols, managing study budgets, and ensuring compliance with applicable regulations and guidelines. The Initiation Clinical Research Associate II is also responsible for coordinating and managing the activities of the study team, including the clinical research staff, investigators, and other stakeholders. Job Skills Required
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Excellent organizational and project management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to manage multiple projects simultaneously
Job Qualifications
• Bachelor’s degree in a related field
• At least 3 years of experience in clinical research
• Certification in clinical research (e.g. CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Knowledge of clinical trial design and data management
• Knowledge of Good Clinical Practice (GCP)
Job Experience
• At least 3 years of experience in clinical research
• Experience in managing clinical research studies
• Experience in coordinating and managing the activities of the study team
Job Responsibilities
• Develop and execute study protocols
• Manage study budgets
• Ensure compliance with applicable regulations and guidelines
• Coordinate and manage the activities of the study team
• Monitor study progress and ensure data accuracy
• Prepare and submit study reports
• Provide training and guidance to study team members