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Remote Clinical Research Associate Jobs in Fremont, Iowa

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
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.
Clinical Controls Manager - Legal/Clinical Research (Remote)
By Stryker At , Fremont, 94538, Ca $95,100 - $204,000 a year
Current and working knowledge in interpretation/implementation of government and other local state/government regulations/requirements governing the ability required
Manage programs/projects, defining milestones and success criteria, resource allocation and successful on-time delivery.
Negotiate, structure, and manage clinical contractual documents that establish business relationships with vendors, customers and/or partners.
Coordinate, manage, and facilitate business processes to provide timely deliverables.
Provide training and overall guidance to on the clinical affairs organization on contracts and financial requirements.
6+ years of applicable experience in legal contracts, conducting business/financial negotiations, and other binding agreements required
Administrative Assistant - Clinical Research Publications (Remote)
By The American College of Radiology At , Remote $21.62 - $28.85 an hour
Format manuscripts according to journal-specific requirements
3+ years of medical/healthcare administrative support experience preferred
Excellent written and verbal communication skills
Superior writing and editing skills
Excellent organizational skills with attention to detail
Ability to successfully manage multiple projects from conception to completion, working in a team environment.
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 - 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 (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 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/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 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 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 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

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and