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Clinical Research Associate 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)
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
Senior Clinical Research Associate (Usa)
By Premier Research At , Remote
4+ years of independent on-site monitoring experience with all types of site visits
We are Built by You. Your ideas influence the way we work, and your voice matters here
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
You must live in United States
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.
Clinical Trials Research Associate - Gastroenterology/Hepatology
By The University of Iowa At , Iowa City, Ia
Protocol Development/ Management and Study Responsibilities:
Excellent time management skills and the ability to perform detail oriented work independently is required
Experience with following specific protocol techniques and management is desirable.
Manage and organize regulatory documentation from sites and regulatory authorities.
Manage and organize regulatory documents from sponsors and CROs.
Excellent written and verbal communication skills are required.
Senior Clinical Research Associate
By Premier Research At , Remote
Must have at least 6+ years of independent monitoring experience
Must have knowledge of applicable clinical research regulations (FDA, GCP, ISO)
Must have direct sponsor experience at a pharma or biotech
Strong communication and organizational skills required
Ensures monitoring, monitoring report review/finalization, event reporting and all other monitoring commitments are performed in accordance with the study monitoring plan.
Conducts a thorough comparison (monitor) of case report forms against medical records on complex trials at multiple sites.
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 Associate - Medical Device
By Meridian Bioscience, Inc. At , Remote
Interact with data management and study sites with generation and reconciliation of queries in order to meet business timelines
Provide answers to common protocol study related questions under the supervison of the Clinical Director or Associate Trial Manager
Assist in the identification and qualification of study sites
Minimum of 3 years experience as a CRA
Preferred: minimum of one year research and development experience
Basic knowledge in the areas of microbiology, immunology or molecular biology and biochemistry as related to infectious diseases
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 Ll-Lll- Vaccines - Home-Based (Us) - Florida Region
By ICON At , Remote
Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms
Applies knowledge of ICON’s policies and procedures
Demonstrates excellent knowledge of ICH/GCP
Displays ability to manage investigative sites to facilitate trial deliverables
2 years of experience supporting clinical trials. No In-House or site level experience will be considered
Advanced skill in utilization of applicable clinical systems
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 - Home-Based (North East, Usa)
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 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
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
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
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
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 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
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
Clinical Research Associate/Site Manager
By Relmada Therapeutics, Inc At United States
·3+ years of clinical monitoring or site management experience.
Delivers high quality and timely reports following each site management or site monitoring visit.
May include managing query resolution process with clinical sites and data management groups.
·Thorough knowledge and understanding of ICH/GCPs and applicable regulatory requirements.
·Solid computer skills, including working knowledge of Microsoft Office applications (Word, Excel Outlook, etc.).
Prepares for and conducts site qualification and site initiation, visits. May also include interim and closeout monitoring visits.
Associate Clinical Research Coordinator
By Rush University Medical Center At , Chicago, 60612

Job Title: Associate Clinical Research Coordinator Department: Psychiatry Admin Shift: 1st Specialty: Research Job Number: 2023-2846 Date Posted: 08/08/2023 Position Type: Research Job ...

Clinical Research Associate Jobs
By Candel Therapeutics At , Needham, 02494
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Clinical Research Associate Jobs
By Balt USA At , Irvine
Experience in clinical study management required.
Manages Trial Management Filing (TMF) system, including document inspection, filing, and auditing.
Serves as key facilitator and liaison for shipping, receiving, and management of study devices.
Ability to constructively interact directly with senior management teams.
Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.
Manages study and site materials, including, but not limited to study binders, study trackers, training documentation.
Associate Clinical Research Coordinator - Cbru
By Mayo Clinic At , Jacksonville, 32224 $22.91 - $33.27 an hour
Preference given to candidates with the following qualifications:
Sincere interest in promoting research within local underrepresented communities.
Affirmative Action and Equal Opportunity Employer
Clinical Research Associate Jobs
By Vial At San Francisco, CA, United States
Site management and monitoring activities across all US clinics
Minimum of 2 years work experience as a Clinical Research Associate
You should be life science degree educated with independent on-site monitoring experience.
Flexibility and ability to travel are paramount with strong communication, written and presentation skills.
Must have experience in Dermatology and Ophthalmology studies.
Work with sites to adapt, drive and track subject recruitment plan
Clinical Research Associate - Mid-West/Central - Cns/Gen Med - Home Based
By Worldwide Clinical Trials At 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
Clinical Research Associate (Fsp) - Poland
By Parexel At United States
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Excellent time management and social skills
Minimum of 2 years of active independent field monitoring experience - all types of visits.
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.
Benefits Of Working With Parexel FSP

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Associate to join our team and help us develop and execute clinical studies. You will be responsible for managing clinical trials, ensuring compliance with applicable regulations, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview:

A Clinical Research Associate (CRA) is a healthcare professional who works in clinical research and is responsible for monitoring the progress of clinical trials. The CRA is responsible for ensuring that clinical trials are conducted in accordance with the protocol, applicable regulations, and ethical standards.

Detailed Job Description:

A Clinical Research Associate is responsible for the planning, coordination, and execution of clinical trials. This includes the development of study protocols, the selection of clinical sites, the recruitment of study participants, the collection and analysis of data, and the reporting of results. The CRA is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and ethical standards.

What is Clinical Research Associate Job Skills Required?

• Knowledge of clinical research principles, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Attention to detail and accuracy
• Proficiency in Microsoft Office applications

What is Clinical Research Associate Job Qualifications?

• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Certification as a Clinical Research Associate (CCRA) or Clinical Research Professional (CRCP)

What is Clinical Research Associate Job Knowledge?

• Knowledge of clinical research principles, regulations, and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial design and data analysis

What is Clinical Research Associate Job Experience?

• Previous experience in clinical research or related field
• Experience in monitoring clinical trials
• Experience in data collection and analysis

What is Clinical Research Associate Job Responsibilities?

• Develop and implement clinical trial protocols
• Monitor clinical trial sites to ensure compliance with protocol and applicable regulations
• Recruit and screen study participants
• Collect and analyze data
• Prepare and submit reports to regulatory agencies
• Maintain accurate and up-to-date records
• Ensure the safety of study participants