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Initiation Clinical Research Associate Ii Jobs

Clinical Research Coordinator Ii
By Ann & Robert H. Lurie Children's Hospital of Chicago At Streeterville, IL, United States
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Student loan servicing and support
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children’s facilities
Clinical Research Associate Ii (Home-Base)
By Talentify.io At United States
Utilize systems and technology for account management tasks
Remote work-from-home position with flexible schedules
Comprehensive benefits package including medical, dental, vision, and life insurance
Excellent communication skills, both written and oral
Basic knowledge of Microsoft Office Suite and Windows operating system
Strong problem-solving and conflict resolution skills
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 (Scientific)
By Akkodis At Waltham, MA, United States
3-5 years of relevant research experience in a biopharmaceutical setting in immunology, biology, chemistry, biochemistry, genetics, or related field.
No Postdoc experience required but preferred.
Benefits include but are not limited to:
Bachelors Degree in biology, chemistry, biochemistry, genetics or related field plus
Comprehensive medical insurance (PPO, HSA)
Three weeks of Paid Time Off to Start; Accumulating Structure Afterwards
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.
Clinical Research Coordinator Ii-Msh-Cs03-12118-013
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
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 Rutgers University At New Brunswick, NJ, United States
Experience with qualitative research methods such as content analysis.
Experience with SAS and SPSS statistical software and Qualtrics or Survey Monkey software.
Additional related experience may be substituted for the degree on a year-for-year basis.
Performs various research activities related to tobacco; may conduct independently or as assigned specialized research for a particular project.
Assists in the implementation of the programs and projects in special areas of interest to the department.
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, Hpv Genomics Team, Cgr
By BioSpace At Rockville, MD, United States
In addition to the education requirement, a minimum of five (5) years of progressively responsible biomedical experience
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below
Support process improvement and assay development activities in collaboration with CGR development resources and senior laboratory management staff
Strong organization skills, ability to multitask and manage time effectively
Critical thinking skills and ability to identify, document and analyze important variables in an experiment
Excellent communication skills (verbal and written)
Clinical Research Associate Ii
By Reflow Medical At United States
SPECIAL SKILLS, ABILITIES, AND REQUIREMENTS
Coordinates and manages the activities of investigative sites to ensure compliance with study protocol requirements
Supports device management, including device accountability, at the site and Sponsor level
Advanced knowledge and experience with GCP/ICH and local regulations
Experience in web-based data collection applications, knowledge of key areas of Compliance
Previous field monitoring experience required, monitoring of device trials in the cardiovascular space preferred
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
Clinical Research Associate Ii, Oncology, East Coast Us Home-Based, Iqvia Biotech
By IQVIA At Durham, NC, United States
Effective time and financial management skills.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Requires at least 1 year of on-site monitoring experience.
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Clinical Research Coordinator Ii-13400-043
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Sr. Research Associate Ii
By Takeda At Boston, MA, United States
Develop intricate experimental protocols and advance the project while internally analyzing, interpreting, and reporting findings to managers and project teams.
Previous experience working in lab setting.
Experience with non-viral gene delivery systems using EP, cell transfection, virus transduction, and CRISPR gene editing is strongly preferred (Electroporation).
Experience with CliniMACS Prodigy, CliniMACS plus, LOVO, or Sepax is a plus.
Implement project assignments in conjunction with coworkers and departmental teams, taking ownership of the technical components of the task.
Use your expertise in laboratory technology to mentor and educate junior personnel while collaborating with other departments and colleagues on projects.
Research Associate Ii, Human Brain Variation Project
By Broad Institute of MIT and Harvard At Cambridge, MA, United States
Experience generating single-cell RNAseq, ATACseq, and multiome data preferred but not required.
Excellent written and verbal communication skills.
Optimize and execute molecular-biological reactions such as PCR, DNA extractions from human brain tissue, and next generation sequencing (NGS) library preparation
Maintain meticulous records and document all experiments in the lab notebook
Attend and contribute to team meetings
Contribute to generation and optimization of experimental protocols
Clinical Research Coordinator Ii-Psychiatry - Ism - Ft - Day
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
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
Sr. Clinical Research Associate Ii
By Labcorp At , Durham, 27703, Nc $120,000 - $155,000 a year
Advanced site monitoring; study site management; and registry administration skills.
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 and clinical trial reports as assigned
Food And Climate Research Associate Ii
By World Resources Institute At , Remote $96,000 - $116,000 a year
Project management end-to-end of research projects
Proven track record of management of research projects and multi-disciplinary research teams
Experience communicating to multiple audiences, including academics, practitioners, business managers, and policy makers
Where appropriate, manage contractors and/or external research contributors
Manage engagement with internal and external partners
Minimum of 7 years full-time relevant work experience conducting independent research, analysis, and publication on related topics

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