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Remote Clinical Research Associate Jobs in Massachusetts

Research Associate - Remote | Wfh
By Get It Recruit - Educational Services At Boston, MA, United States

Are you ready to embark on a journey of intellectual curiosity and creative exploration? We're on the lookout for a passionate and driven individual who thrives in a collaborative, high-energy ...

Clinical Research Associate Jobs
By Candel Therapeutics At Needham, MA, United States
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Clinical Research Associate Jobs
By Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...

Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics
By Moderna At Norwood, MA, United States
Identify and resolve quality issues and report issues to upper management
Good computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism
Conduct assay development, qualification/validation and sample analysis on a variety of platforms (ELISA, MSD, Ella, Automated ELISA Workstation etc.)
Assume assigned general laboratory responsibilities, e.g., safety coordinator, instrument/process/technology owner etc.
Bachelor or MSc in bioanalysis or related field with immunoassay experience preferably in a regulated environment
Good written, presentation, and interpersonal communication skills
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 Associate Jobs
By Aequor At Waltham, MA, United States
Experience in operation of multiple flow cytometry platforms (e.g.: Client, Sony, etc.) and specialized analysis software (e.g.: FlowJo, ...)
Previous experience with flow cytometry, hands-on experience in developing flow cytometry-based methods.
Hands-on experience with gene editing technologies is a plus.
Prior experience with the following is preferred
Cell isolation, sample preparation and staining
Must be proficient in cell-based assay development and molecular techniques.
Clinical Analyst - Remote!
By Queen Consulting Group At Quincy, MA, United States
· Advises senior analysts and/or managers of potential problems, requirements for expanded services, and status of current systems
· Builds, tests, and debugs Epic applications(s) to ensure the system meets end user requirements
Location: Must live in MA, RI, NH but can be remote!
Salary - up to 110K depending on level of experience
· Prepares functional and technical software specifications
· Designs, validates, and confirms new or changed functionality with the Epic environment
Senior Clinical Research Associate
By Alexion Pharmaceuticals, Inc. At Boston, MA, United States
Training, supporting, and advising Investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles.
Excellent understanding of Clinical Study Management including monitoring, study drug handling and data management.
Minimum of 4 years of CRA monitoring experience
Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
Excellent knowledge of relevant local regulations.
Clinical Research Associate Jobs
By Digital Prospectors At Cambridge, MA, United States
Good conflict management and negotiation skills.
Attend qualification and site initiation visits.
Assist the Clinical Trial Manager in the review of ICFs and essential documents.
Track clinical supply shipments and manage shipment logistics.
Strong communication skills both verbally and written in English.
Minimum of 2-3 years demonstrated site monitoring experience in a biotechnology, pharmaceutical, and/or CRO company.

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and