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Research Associate Clinical I Jobs in Story, Iowa

Clinical Research Associate Jobs
By Philips At , Cambridge
Shipping/ labeling/Site Management and Team meeting facilitator
Database Lock (listing review as needed/ Data query & resolution/Source data verification – onsite or remotely)
Read more about our employee benefits.
Generation of Study Documents (Clinical Monitoring Plans/ Informed Consents/ data source work sheets/Device accountability/training slides and work instructions)
Site start up to Site Activation (SA) to include Investigator Site File/Inventory and Device
Study Duration (Enrollment tracking/Key Performance Indicators/Adverse Events/ Serious Adverse Events)
Research Associate I Jobs
By The University of Texas Rio Grande Valley At , Remote
May train users on the operation and data management of research equipment.
Collects, compiles, and analyzes research data.
Prepares, collects, evaluates, and verifies samples and supporting records for experiments.
Uses statistical methods and relational databases to analyze data sets.
Prepares or assists with preparing reports of research findings.
Assists with planning, developing, coordinating, and administering research projects.
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 Associate - Sponsor Dedicated
By IQVIA At , Remote
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
Effective time and financial management skills.
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.
Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Clinical/Hc Research Associate
By University of Iowa At Iowa City, IA, United States
Protocol Development/Management And Study Responsibilities
Oversee operations of clinical research studies including the recruitment, coordination, and scheduling of subject participation and procedures per protocol requirements.
Collect and manage data in clinical trials using a variety of data programs including REDCap data capture.
Good Written And Verbal Communication Skills Are Required.
Participate in the development of the general research goals and in the planning and implementation of the clinical trials.
Coordinate services/referrals as appropriate with other departments participating in the clinical research as appropriate.
Senior Clinical Research Associate (Phase I Oncology)
By Premier Research At , Remote
Perform remote monitoring activities for Phase I oncology clinical trials
Must have Oncology experience (Phase I preferred)
4+ years of independent on-site monitoring experience with all types of site visits
Identify and escalate potential risks and possible retraining opportunities for investigative sites.
Bachelor’s degree, or local equivalent, in a clinical, biological, scientific, or health-related field or its international equivalent
Completion of a CRA training program through a CRO
Clinical Research Associate I (Home-Based In Us)
By Syneos Health Clinical At , Remote $55,800 - $93,067 a year
For the Clinical Monitoring/Site Management Plan (CMP/SMP):
Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Must demonstrate good computer skills and be able to embrace new technologies
Excellent communication, presentation and interpersonal skills
Ability to manage required travel of up to 75% on a regular basis
Clinical Research Coordinator I
By Regions Hospital At , Saint Paul, 55101, Mn
Minimum of two years of experience working in a health care setting
Clinical research experience in a clinical, academic, or industry setting.
Bachelor’s degree in a healthcare, medical or science related field
Clinical Research Associate - Home-Based (Southeast)
By ICON At , Remote
Strong interpersonal, collaboration and time management skills
Verifies proper management and accountability of Investigational Product (IP).
In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements
Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
May serve as preceptor, providing training to less experienced clinical team members
2 years of experience supporting clinical trials including 1 year of on-site monitoring experience
Clinical Research Associate - Home-Based (Colorado And Midwest)
By ICON At , Remote

Benefits of Working in ICON:

Clinical Research Associate Iii - Remote
By Orthofix At , Remote
Ensure subject safety in all areas of clinical research, following procedures to report SAEs and UADEs to clinical and regulatory management.
Significant industry experience in clinical research, three to five+ years as a CRA performing field-based monitoring preferred.
Demonstrated knowledge of FDA regulations and ICH – GCP guidelines.
Ability to effectively manage a study from start to finish.
Excellent communication skills required to effectively work with all individuals including the sales force and staff at study sites.
Proficient computer skills using Microsoft Office products.
Clinical Research Associate 2/3 - Biotech
By ICON At , Remote
Knowledge of ICH and local regulatory authority regulations regarding drug trials
Benefits of Working in ICON:
Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health care professional licensure, i.e.
What do you need to have?
Clinical Research Associate Ii
By Labcorp At , Allentown, 18104, Pa $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 Specialist I Jobs
By Princeton University At , Princeton, 08542, Nj

Overview: The Department of Psychology is looking for a Research Specialist to manage the laboratories of Professors Tania Lombrozo and Tom Griffiths. The successful applicant will handle lab ...

Clinical Research Associate (Cra)
By ClinSmart At , Remote
BS/BA in Life Science or Nursing (or equivalent foreign education / experience) required
Perform on-site and remote monitoring activities from study start-up through close-out
Perform all duties and responsibilities in adherence to protocols, FDA regulations, ICH/GCP guidelines, and company / client SOPs
Extensive knowledge of FDA regulations and GCPs
Computer proficient with EDC experience
Excellent verbal and written communication skills
Research Associate I - Social Sciences
By University of Illinois Chicago At Chicago, IL, United States
Job Knowledge & Skills, Education, Experience
Research Associate I- Social Sciences
About The University Of Illinois Chicago
Clinical Research Associate Jobs
By iCell Gene Therapeutics At Stony Brook, NY, United States
At least two years of experience as a clinical research associate
Excellent writing, editing, and communication skills
Strong Administrative and Organizational skills to support several team members
A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences
Familiarity with various computer document formats, styles, and standards
· Collecting, analyzing, and recording data
Clinical Research Associate Jobs
By Integrated Resources, Inc ( IRI ) At Mountain View, CA, United States
The Clinical Research Intern will apply analytical, project management skills and enthusiasm for healthcare and commitment to improving healthcare through research.
The candidate will Product practical experience within the Clinical Research operations at ***.
Complies with established policies, health and safety regulations and requirements, procedures, and department objectives.
Bachelor's Degree in biological or life sciences or health related field OR attending/completed a clinical research certification program.
Proficient computer skills using Microsoft Office products.
May assist with follow up and closing of clinical studies.
Clinical Research Associate Jobs
By Juno Search Partners At Greater Philadelphia, United States
Able to manage multiple and competing priorities through effective organizational management skills.
Effective interpersonal skills; able to build effective relationships with study management team colleagues and business partners.
Excellent time management skills; able to accomplish established goals efficiently.
Supply chain management support may include:
Support Trial Management team member with assigned study specific projects and tasks.
Two years Clinical Research work experience, or relevant experience
Clinical Research Associate Jobs
By Talencio At Greater Minneapolis-St. Paul Area, United States
Clinical Trial Collaboration: Work alongside our clinical team, focusing on site qualification, initiation, management, and data integrity.
Data Management: Oversee data activities, generate, and resolve queries, and report on study metrics including enrollment and adverse events documentation.
Regulatory Oversight: Manage investigational product accountability, monitor IRB requirements, and ensure prompt processing of regulatory documents.
Bachelor’s degree in a medical/scientific field, with 4+ years of clinical research experience (Master’s degree can substitute for 1 year).
Strong organizational, multitasking, and relationship-building abilities.
Effective communication skills and keen attention to detail.
Clinical Research Associate I- Principal
By i-Pharm Consulting At United States
Conduct all types of visits including, qualification, initiaiton, monitoring and close out
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
Minimum 1.5 years monitoring experience
Strong verbal and written communication skills
8-12 days on site per month
Clinical Research Associate Jobs
By Lumicity At Austin, TX, United States
5+ years of CRA experience.
3+ years of experience working on oncology studies.
BS in a relevant scientific discipline.
Ability to travel and be on-site. (Austin, TX or Portland, OR).
6-month contract. - 40 hours per week. - Monday to Friday.
Austin, TX or Portland, OR
Clinical Research Associate - Southeast - Cns / Gen Med - Home Based
By Worldwide Clinical Trials At North Carolina, United States
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
5+ years of experience as a Clinical Research Associate
Experience in CNS is required
Conduct study initiation visits (SIVs)
Ability to work with little or no supervision
Research Associate I - Health Research (Remote) ($70000.00 / Year)
By Talentify.io At United States
Required Knowledge, Skills, And Abilities
Assists with the preparation of summary documents and reports in conjunction with Program Manager and Project Manager.
Strong communication, qualitative and quantitative analytical skills.
Experience within Health Services Research preferred.
Experience in biostatistics and epidemiology.
Minimum of 0-2 years' experience required.
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.
Clinical Research, Data Associate I
By Castle Biosciences, Inc. At Phoenix, AZ, United States
Ability to multi-task and have good organizational and time management skills.
Experience in clinical research or the medical field preferred
Experience with Electronic Data Capture (EDC) systems, for the purpose of clinical research, preferred.
Experience with programming and coding (e.g., HTML and Java) required.
Possess excellent written and oral communication skills.
Critical thinking and problem-solving skills
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).
Ophthalmology Clinical Research Associate
By SRG At United States
Minimum of four (4) years of experience in clinical research specifically in Ophthalmology surgical medical devices.
Experience in glaucoma devices is strongly preferred.
Knowledge of medical and ophthalmology terminology
Remotely monitor data and support clinical sites for protocol compliance and recruitment activities
Manage clinical trial close-out activities, including return of investigational product, final reconciliation of all required documentation, and EDC close-out
** Candidates must have experience in Ophthalmology Clinical Research trials to be considered!
Clinical Research Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
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.
Clinical Research Coordinator I-Iii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3-5 years clinical 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
Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection
Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)
UAMS offers amazing benefits and perks
Clinical Research Associate Jobs
By Brain Tumor Network At Ponte Vedra Beach, FL, United States
• Maintains on-going professional education on clinical trials and research
• Minimum requirement: master’s degree in nursing/Healthcare related field
• Clinical work experience in oncology
• Excellent organizational and communications skills, with team-player proven ability to meet project deadlines
• Knowledge of data analytics
• Serves as a liaison to industry sponsored, consortium and Investigator initiated Brain Tumor Trials
Research Associate I Jobs
By Planet Pharma At South San Francisco, CA, United States
Basic knowledge of analytical chemistry methods Sincere interest in translating basic research insights into impactful therapeutics
Operate and maintain robotic systems for high-throughput assays.
Conduct physicochemical property assays, including but not limited to logD, pKa, and stability tests.
Collect, analyze, and interpret data generated from assays, ensuring high-quality and reliable results.
Maintain accurate and up-to-date records of all experiments and findings.
Assist in troubleshooting equipment and experimental problems.
Research Associate I Jobs
By AcuraStem At Monrovia, CA, United States
B.S. in a biology discipline (Biology, Neuroscience, Bioengineering), 0-2 years of industry experience
Experience in mammalian cell culture
Experience in DNA/RNA extraction, PCR/qPCR, ELISA, western blot, immunostaining
Effective verbal and written communication skills relating to colleagues and associates inside and outside the organization.
Maintain cell lines (hiPSCs/HEK/Glia cell) with sterile techniques.
Support and collaborate with scientists, labs, vendors, and industry experts to ensure the completion of tasks/projects.
Clinical Research Associate Jobs
By AstraZeneca At , Wilmington, 19803
Good understanding of Clinical Study Management including monitoring, study drug handling and data management
1.5+ years of CRA experience in Cardiovascular/Metabolic, Respiratory and/or Immunology therapeutic experience
Fluent knowledge of spoken and written English
Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge in relevant AZ Therapeutic Areas