Clinical Research Leader Jobs
By Indiana University–Purdue University Indianapolis At Indianapolis, IN, United States
Demonstrated time management and priority setting skills
Designs and implements proper data management for data collection and tracking and/or oversee design of such databases.
Expands knowledge base and keep abreast with new research developments by attending continuing education meetings, lectures, training sessions and conferences
Combinations Of Related Education And Experience May Be Considered
2 years of clinical research experience
ACRP or SOCRA Clinical Research Certification upon date of hire
Biostatistician - Epidemiology/Clinical Research - Remote
By WESTAT At , Rockville, 20850, Md $90,000 - $105,000 a year
Participate in all phases of analytical programming, data management, macros, quality control and reporting of research data.
Expert ability to identify and resolve analytic issues using knowledge, background, problem solving and troubleshooting skills.
The anticipated pay for this role is $90-105k and will be commensurate with experience.
Collaborate with external investigators in developing study aims and research hypotheses.
Provide study design advice to investigators including assessment of appropriateness and feasibility.
Develop statistical considerations and analysis methods for study protocols.
Clinical Research Assistant Jobs
By Children's National Hospital At , Rockville, 20850, Md
Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
Meets all annual job-related training and compliance requirements.
Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
Identifies participants that meet eligibility requirements under the supervision of a senior research team member.
Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.
Consistently demonstrates adherence to the standards for the responsible conduct of research.

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