Sr. Clinical Research Associate (100 % Remote)
By Thrive At Cambridge, MA, United States
Assist with essential documents collection, review and archiving (TMF management)
Provide project management support for PTX project team, including vendor oversight
Conduct Site Initiation, Routine, and Close-out monitoring site visits, either on-site or remotely, prepare visit correspondence and records including trip reports
Oversee the conduct of assigned study sites, including ensuring compliance with SOPs, federal and local regulations, and ICH and GCP guidelines
Assist in the review and /or development of clinical trial documents such as study plans and training materials
Participate in and assist with facilitation of project team meetings
Clinical Research Coordinator Jobs
By Alcanza Clinical Research At Methuen, MA, United States
May participate in community outreach / education events;
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, and supplemental insurance are offered.
Screening of patients for study enrollment;
Documenting in source clinic charts;
Clinical Research Coordinator Jobs
By Alcanza Clinical Research At Boston, MA, United States
May participate in community outreach / education events;
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, and supplemental insurance are offered.
Screening of patients for study enrollment;
Documenting in source clinic charts;
Clinical Research Coordinator I With Transplantation
By Beth Israel Lahey Health At Burlington, MA, United States
Implements assigned research studies by reviewing study and assessing protocol and institutional requirements:
Ensures appropriate training and certification for all members of the study team involved in the research protocol.
Works collaboratively with research finance to process clinical trial agreements, study budget development and other finance issues, as applicable.
Conducts assigned research studies per protocol requirements, departmental and institutional policy:
Participates in and actively seeks continuing education opportunities.
Maintains required continuing education credits per institutional and departmental SOPs.

Are you looking for a rewarding career in clinical research? We are seeking a Remote Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, ensuring compliance with regulatory standards, and providing support to research teams. If you are passionate about making a difference in the medical field, this is the perfect opportunity for you!

Overview A Remote Clinical Research Coordinator is responsible for coordinating and managing clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. Detailed Job Description The Remote Clinical Research Coordinator is responsible for the coordination and management of clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. The Remote Clinical Research Coordinator is also responsible for the development and implementation of research protocols, the collection and analysis of data, and the preparation of reports and presentations. The Remote Clinical Research Coordinator must be able to work independently and collaboratively with other team members. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to work independently and collaboratively
• Excellent organizational and communication skills
• Proficiency in data analysis and reporting
• Ability to manage multiple projects simultaneously
• Knowledge of computer systems and software
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Knowledge of Good Clinical Practice (GCP)
• Ability to work in a remote setting
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of computer systems and software
Job Experience
• At least two years of experience in clinical research
• Experience in data analysis and reporting
• Experience in project management
Job Responsibilities
• Develop and implement research protocols
• Collect and analyze data
• Prepare reports and presentations
• Manage multiple projects simultaneously
• Ensure compliance with clinical research protocols and regulations
• Communicate with clinical research teams, sponsors, and other stakeholders
• Work independently and collaboratively with other team members