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Initiation Clinical Research Associate Ii Jobs

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
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 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
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.
Research Associate Ii - Social Sciences
By University of Illinois At , Chicago, 60612, Il
1019862- Research Associate II- Social Sciences
About the University of Illinois Chicago
This position conducts research by assisting with the collection, entry and cleaning of data and descriptive results.
Required Employment Notices and Posters
The university provides accommodations to applicants and employees.
Research Associate Ii Jobs
By Mindlance At Waltham, MA, United States
Experience in mammalian cell culture is required.
Excellent organizational and communication skills.
Duration- 12 months contract (Possibility of extension)
Independently design and conduct experiments to improve AAV vector productivity and quality.
Record experimental procedures and data in the Electronic Lab Notebook (ELN) in a timely manner.
Contribute to a safe, efficient, and effective laboratory environment.
Research Associate Ii - Postsecondary Education Research
By NORC at the University of Chicago At , , Or
Strong writing skills, including experience with report writing.
Experience working with data, conducting data quality review and data analysis. Additional advanced quantitative research skills.
At least 18 months of relevant work/social science research experience.
Experience with or training in the principles, processes, and methods of social science research a plus.
Outstanding interpersonal and critical reasoning skills.
Experience conducting interviews and/or focus groups.
Clinical Research Coordinator Ii (Multiple Vacancies)
By Rutgers University At New Brunswick, NJ, United States
Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
This role requires strong organizational and prioritization skills, as the coordinator will be responsible for managing 4 to 5 concurrent trials.
Excellent interpersonal skills are essential for clear and confident patient interactions.
Experience in cardiology and complex clinical trials is a plus.
Physical Demands: Standing, sitting, walking, talking or hearing. No special vision requirements. Lifting (up to 25 pounds).
Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines.
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 Coordinator Ii
By Roswell Park Comprehensive Cancer Center At Buffalo, NY, United States

Title: Clinical Research Coordinator II Job Type: Regular Company: Health Research Inc. Department: Clinical Research Services Time Type: Full time Weekly Hours: 40 Shift: First Shift (United States ...

Research Associate Ii, Core Technologies, Cell Analytics
By Astellas Pharma US At Seattle, WA, United States
Strong organizational, time management skills, and the ability to maintain accurate and up-to-date records.
Excellent communication and interpersonal skills.
Experience with pluripotent stem cell culture techniques.
Experience performing assays within a Quality Assurance framework
Experience designing, troubleshooting, and optimizing cell-based assays
$64,500 – $86k (NOTE: Final salary could be more or less, based on experience)

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