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Clinical Research Jobs in Union, Arkansas

Clinical Research Analyst *Remote*
By Talentify.io At United States
Communicate extensively with various stakeholders to manage research activities including billing compliance, budgeting, subject tracking, data collection, and sponsor invoicing.
Bachelor's Degree in a health-related field or 4 additional years of related experience.
Three years of IRB, regulatory, or research experience (4 years preferred).
Three years of relevant CTMS experience.
This is a remote position that can be based in any Providence state approved location in the US.
Review clinical research protocol documents and replicate the protocol schedule of events in Velos EResearch CTMS.
Clinical Research Manager Jobs
By Masis Professional Group At United States
Minimum of 5 years' experience working in a Clinical Research Manager or Clinical Project Manager role with relevant experience.
Experience with FDA and US requirements for the conduct of clinical studies is a must.
Multi-disciplinary international project management managing diverse relationships.
Exciting job opportunity with project responsibilities and freedom for professional growths and acquisition of new skills
Supervision (remote and in-person) of participating study centers
Ability to manage multiple projects in parallel and prioritize across study, regulatory, and company goals.
Clinical Research Coverage Analyst - 198571
By Medix™ At United States
● Knowledge of clinical research protocol management.
Job Summary & Preferred Qualifications:
● Certification in Health Research Compliance preferred.
● Knowledge of clinical research budgeting.
● Creates coverage analysis grids.
● Researches and applies policies, guidance and guidelines from various sources including federal and state regulations.
Clinical Research Engineer Jobs
By OrganOx At United States
· Knowledge of project management tools and practices
· Experience with perfusion devices and management of patients or donor organs is a must
· Identify and report study protocol challenges and compliance issues to clinical management
Responsibilities may include the following and other duties may be assigned:
· Experience in a clinical setting and clinical studies is beneficial
· Excellent presentation and computer skills
Clinical Research Monitor (Remote, Southwest Region) Tmtt
By Edwards Lifesciences At Pueblo-Cañon City Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Clinical Research Coverage Analyst - 205830
By Medix™ At United States
Knowledge of clinical research protocol management.
Certification in Health Research Compliance preferred.
Knowledge of clinical research budgeting.
** Remote Medicare Coverage Analyst!! **
**Must have Clinical Research Experience**
Researches and applies policies, guidance and guidelines from various sources including federal and state regulations.
Research Analyst - Clinical Research - Remote
By Talentify.io At United States
Strong organizational and time management ability.
Manage the study website, update content, and respond to queries from external investigators and NIH clients.
Prepare documents and power points, draft reports, and manage IRB submissions for multiple sites.
Minimum of 2 years of job experience in clinical/scientific research.
Excellent communication and collaboration skills.
Support research committees by organizing virtual and in-person meetings, preparing agendas, materials, meeting minutes, and action items.
Clinical Research Scientist Jobs
By Target ALS At United States
Manage creation of complex sample management plans to ensure proper collection and storage of samples for analysis.
Oversee LIMS system in coordination with core programmanager. Collaborate with sites to streamline and codify data entry for LIMS system.
Ensure utilization of NIH Common Data Elements into the data management scheme
Collaborate with the Grant funded Biofluid and Post-mortem core facility investigators to manage and drive growth of these core resources.
Manage Target ALS diversity initiative aimed at increasing participation of rural, under-represented and minority communities in ALS research.
Manage the biosample and dataset request approval system for Target ALS Cores.
Clinical Research Specialist Jobs
By Roth Staffing At United States
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Must have knowledge in reference to good clinical practices regulations and standard operating procedures.
The job requires the ability to make judgements based on practice and previous experience.
Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.
Clinical Research Education & Training Manager
By EmVenio Research At United States
Advanced organizational and project management abilities, including the ability to work within tight deadlines on a range of projects.
Identifies knowledge gaps to improve efficiency and reduce time to proficiency.
Bachelor’s degree or equivalent experience is required.
Demonstrated leadership skills, including strong communication, presentation, written and interpersonal skills.
Basic non-investigator clinical skills related to site research roles required.
Strong analytical and decision-making capabilities that support clinical improvement initiatives.
Clinical Research Coordinator I - Light & Health Research Center
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Client Partner, Clinical Research
By Verily At United States
15+ years of relevant experience in Enterprise sales or business development focused on SaaS, Real Word Data and/or scientific services.
Experience selling complex solutions and driving significant revenue growth.
Proven ability to work with complex, technical software and service offerings, and processes involving multiple stakeholders.
Experience with Google suite of productivity applications (gMail, gCalendar, Sheets, Slides, Docs).
Build and maintain strong relationships with customers and partners.
Focus on transformational outcomes that make an impact for patients, clinical investigators and the life sciences companies we serve.
Clinical Research Fellow Jobs
By Worldwide Clinical Trials At United States
Superb verbal, written, and presentation skills are mandatory.
The position is remote-based. Travel to Texas once a month is required
Preparation of articles, white papers, and webinars as well as assistance and protocol and program design.
Ability to learn to master the art of clinical trials.
Eagerness to accept instruction and learn.
An interest and capability in developing expertise in all phases of clinical research is mandatory.
Clinical Research Assistant Jobs
By Evon Medics, LLC At Washington DC-Baltimore Area, United States
Relationship building and management skills
Experience organizing and facilitating engaging community-based events and activities
Experience engaging and enrolling participants of diverse backgrounds into research studies and Clinical Trials
Excellent communication, presentation, public speaking, and interpersonal skills
Minimum 2-year experience working in a scientific research organization or clinical trials
Student mentality, strong listening, organizational, multi-tasking, and interpersonal skills
Clinical Research Sub Investigator - 211452
By Medix™ At Fayetteville, NC, United States
Provides medical management of adverse events as appropriate
Performs all job responsibilities in accordance with standards of Good Clinical Practice
Delegates study responsibilities as appropriate to trained study staff
Possesses a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form
Performs all study responsibilities in compliance with the IRB approved protocol
Completes all study documentation in accordance with the study specific requirements
Clinical Research Lab Specialist
By AnMed Health At Anderson, SC, United States
Excellent computer and electronic database management skills.
Must possess excellent communication and interactive skills (both verbal and written), while also remaining flexible in responsibilities and work schedule.
Must maintain current certification for compliance and hazardous transport (IATA training).
Clinical Research Nurse Jobs
By Vitalief Inc. At New Brunswick, NJ, United States
Bachelor’s Degree in Nursing preferred. Equivalent education, experience and/or training may be substituted for the degree requirement.
Two or more years of nursing experience working in a hospital setting.
Minimum of 1 year or more years of experience working in an Oncology specialty area in a hospital or clinic setting.
Minimum of 6 months of clinical research nursing experience.
Maintains active Basic Life Support (BLS) certification.
Must possess excellent communication and interpersonal skills to interact with subjects in a clear and confident manner.
Clinical Research Specialist, (Irvine)- Thv
By Edwards Lifesciences At Irvine, CA, United States
Experience in clinical site monitoring, site qualification, and site educational training
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Experience in Medical device trial
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 Finance Manager - Office For Clinical Research
By Emory University At , Atlanta, 30322
Performs related responsibilities as required.
This is a central university department job, reporting to the Office for Clinical Research (OCR).
Under direct supervision, performs a detailed analysis of all industry clinical trial accounts for invoicing, accounts receivable, and accounts payable.
Assists with audit tasks on study assignments.
May perform budget entry in ERMS.
Clinical Research Scientist Jobs
By Seattle Childrens Hospital At , Seattle, 98105 $89,794 - $134,680 a year
Minimum of four (4) years of related research experience.
Advanced degree in scientific related field (Master's, PhD, MD).
Min to Max Annual Salary$89,793.60 - $134,680.00 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Seattle Children's is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.

Are you looking for a career that combines your passion for science with the opportunity to make a real difference in people's lives? Join our team as a Clinical Research Associate and help us develop treatments that will improve the lives of patients around the world!

Overview of Clinical Research Clinical research is a field of healthcare science that focuses on the evaluation of new medical treatments, drugs, and devices. Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. Detailed Job Description of Clinical Research Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. They must ensure that all research is conducted in accordance with ethical and legal standards. Clinical research professionals must also be able to communicate effectively with other healthcare professionals, patients, and sponsors. Clinical Research Job Skills Required
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Ability to analyze and interpret data
• Ability to communicate effectively
• Ability to work independently
• Attention to detail
• Problem-solving skills
• Computer skills
Clinical Research Job Qualifications
• Bachelor’s degree in a related field
• Master’s degree in a related field
• Certification in clinical research
• Experience in clinical research
Clinical Research Job Knowledge
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Knowledge of clinical research regulations
• Knowledge of data analysis techniques
Clinical Research Job Experience
• Experience in clinical research
• Experience in data analysis
• Experience in project management
• Experience in report writing
Clinical Research Job Responsibilities
• Design and conduct clinical trials
• Collect and analyze data
• Report results
• Ensure compliance with ethical and legal standards
• Communicate effectively with other healthcare professionals, patients, and sponsors
• Monitor patient safety during clinical trials
• Prepare and submit reports to regulatory agencies