Clinical Research Scheduler Jobs
By UCLA Health At , Los Angeles, 90095 $26.99 - $38.66 an hour

Description Join our team at the Department of Molecular and Medical Pharmacology as a Clinical Research Scheduler and play a vital role in scheduling and coordinating clinical research ...

Clinical Research Coordinator/Research Audiologist
By Duke University At , Durham, 27710
Enters and collects data, and develops data entry or collection SOPs or tools.
Recognizes and reports security of physical and electronic data vulnerabilities.
Uses systems and system reports to manage research participants activities and charge routing.
Required Qualifications at this Level
Screen participants for complex studies (e.g., procedural and interventional studies).
Develops or helps develop SOPs.
Clinical Research Assistant_Research
By Planned Parenthood GNHI At , Tacoma
Uses ASANA software for project management and organization.
Experience administering informed consent in a research or medical setting.
Experience with electronic medical records systems (NextGen preferred)
Experience with electronic data captures systems.
Experience interacting with patients in a medical setting or research subjects in person.
Recruits, screens, and schedules potential research subjects for studies.
Clinical Research Monitor (Remote) Tmtt
By Edwards Lifesciences At Albuquerque-Santa Fe Metropolitan 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 Compliance Manager
By Weill Cornell Medicine At , New York, 10022, Ny $101,600 - $125,400 a year
Demonstrated organizational skills and ability to pay close attention to detail.
Demonstrated critical thinking and analytical skills.
Demonstrated knowledge of database, word processing, and spreadsheet programs.
Title: Clinical Research Compliance Manager
Approximately five years of prior experience in a clinical research setting.
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Clinical Research Grader Jobs
By SGS At , Richardson, 75081, Tx
Reasoning Skills / Abilities: Basic level
3+ years of relevant experience in industrial or laboratory, or field services setting with experience following strict safety standards. (Required)
Language Skills: English - Advance level
Advances communication skills and ability to interact with paid panelists.
Sets up and conducts studies in compliance with protocols, SOPs, applicable regulations and GCPs.
Performs clinical grading to assess a variety of skin assessments on panelists in a clinical setting.
Clinical Research Nurse Jobs
By Eastside Research Associates At , Redmond, 98052, Wa $50 - $65 an hour
Strong organizational and time management skills
Ensure strict compliance with established research protocols and standards along with all applicable laws, regulations, policies, and procedural requirements
Follow established SOPs, GCP and other applicable regulatory requirements in the execution of all research activities.
Minimum 2 years of nursing experience
Excellent written and verbal communication skills
Knowledge of clinical research operations, including Good Clinical Practice guidelines is preferred
Clinical Research Analyst Jobs
By Intellectt Inc At Alameda, CA, United States

Position Summary The CRAII/Sr. CRA will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of ...

Clinical Research Nurse Jobs
By UC Irvine Health At , Orange, Ca $56.01 - $76.89 an hour
Bilingual skills to communicate effectively with patients and families Understanding of JCAHO requirements
1 year of outpatient and inpatient clinical nursing experience in adult acute care
• Clinical Research Certification • Basic Life Support • Advanced Cardiac Life Support
Background Check and Live Scan
Legal Right to work in the United States
California Child Abuse and Neglect Reporting Act
Manager, Clinical Research Nursing Operations
By Lightship At , Remote $130,500 - $165,000 a year
Strong leadership and performance management skills, including coaching, mentoring and developing nursing talent
At least two (2) years nursing supervisory experience or general people management experience
Required knowledge, skills & abilities:
Managing, mentoring, and developing nursing staff, by providing necessary coaching and overseeing performance management to build high performing team
Knowledge of medical terminology, drug calculation skills, and clinical medicine
Bachelor of Nursing or another Science degree preferred, or requisite combination of education, training, and experience
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 Manager Jobs
By OSF Saint Francis Medical Center At Peoria, IL, United States

Strong leadership abilities to lead an innovative research program.

Clinical Research Specialist Jobs
By Mindlance At Irvine, CA, United States
• Demonstrated experience in establishing and maintaining effective relationships with management, peers and subordinates and customers.
5) What are the top 5 skills/requirements this person is required have?
• Manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges.
a. Required Skill 1: Organized and great attention to detail
b. Required Skill 2: Strong communication skills and intrapersonal skills
c. Required Skill 3: Takes initiative and works well alone and also within a team
Clinical Research Project Manager
By Proper Career Solutions At Los Angeles, CA, United States
• MT Group is a CRO for biospecimen sample acquisition and management
1+ years experience in any of the following:
• 2+ years of experience in a science, research, or medical setting
• Full Benefits (Medical, Vision)
As a research coordinator or research associate
• Small, Growing Company (30 people)
Clinical Research Regulatory Manager
By MBO Partners At Charlotte, NC, United States
5-10 years of clinical trial regulatory management experience.
Quality Management System/Regulatory Compliance Program
5 Years minimum regulatory experience in clinical trials
Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Experience gained from multiple perspectives: industry sponsor, CRO, academic, government or site level
Has GCP training and follows GCP guidelines and other guidelines related to the conduct of human subject’s research
Clinical Research Coordinator - Clinic Research
By St. Luke's Duluth, MN At Duluth, MN, United States
Experience: Experience in healthcare required.
Licensure/Certification/Registration: Current licensure in Minnesota to practice as registered nurse or physician.
Education: Bachelor’s degree in nursing or other field. Course work in research methods, statistics and other related subject matter.
Experience: Experience in clinical research and/or other experience in research field.
Licensure/Certification/Registration: Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP).
WRITING - Intermediate: Ability to write routine reports, correspondence, or procedures.
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 Operations Specialist
By Fred Hutch At Seattle, WA, United States
Experience with Clinical Trials Management System (i.e., OnCore, Velos, etc.)
Organize and manage time and tasks independently
2 years of health care operations experience preferably in clinical research
Demonstrated skills in critical thinking and problem solving
Strong written and verbal communication skills
2 years of clinical research experience
Clinical Research Scientist Jobs
By BioSpace At Arlington, VA, United States
Excellent organization, time management, ability to meet deadlines
Excellent oral, written, and interpersonal communication skills
3-5 years of clinical research experience required
Prior biomedical device development experience preferred
Work closely with the Medical Director and Clinical Research leader (as needed)
Assist to execute the clinical trial as indicated in the clinical development plan (CDP)

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