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Clinical Research Jobs in Massachusetts

Research Assistant (Clinical Research)
By Joslin Diabetes Center At Boston, MA, United States
Experience with routine clinical and laboratory procedures preferred.
Phlebotomy certification – or willingness to become certified on the Joslin Clinical Research center
Ability to perform basic phlebotomy skills, including drawing blood, preferred.
In absence of PI, perform managerial duties.
Working closely with the Office of Sponsored Research and Finance departments, provide oversight of lab financials and assist with budget planning.
Minimum 2 years’ supervisory experience.
Clinical Research Scientist Jobs
By SRG At Boston, MA, United States
Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports
Maintain strong understanding of evolving post-market evidence requirements under EU Medical Device Regulation.
Previous experience developing strategies to generate clinical evidence is strongly preferred
Develop and write high quality Post-market Clinical Follow-up PMCF plans and reports with minimal supervision.
ED&I: Impellam Group and its brands are equal opportunity employers committed to diversity and inclusion.
Clinical Research Assistant Jobs
By Beth Israel Lahey Health At Boston, MA, United States
Independence of Action: Ability to follow general instructions and procedures as provided. Work is monitored by supervisor/manager.
Bachelor's degree required. Master's degree preferred.
Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
Oral Communications: Ability to comprehend and converse in English to communicate effectively with medical center staff, patients, families and external customers.
Physical Nature of the Job:

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