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Remote Clinical Research Associate Jobs in New York

Clinical Research Associate Jobs
By iCell Gene Therapeutics At Stony Brook, NY, United States
At least two years of experience as a clinical research associate
Excellent writing, editing, and communication skills
Strong Administrative and Organizational skills to support several team members
A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences
Familiarity with various computer document formats, styles, and standards
· Collecting, analyzing, and recording data
Research Associate (Remote Or Hybrid)
By Moody's Corporation At New York, NY, United States
Excellent writing, presentation, project management and interpersonal skills are required.
The ideal candidate would have a BA degree in Finance, Statistics or Economics.
Ability to communicate technical subject matter clearly and concisely to individuals from various backgrounds is a plus.
Clinical Research Associate-208919 Jobs
By Medix™ At Florida, United States

The CRA is expected to work cooperatively with study team and operations management to proactively drive project success.

Clinical Research Associate Jobs
By Infobahn Softworld Inc At New York, NY, United States
• Responsible for study-related contracting, budgets, and vendor/partner management
- 3-5 years HEOR modeling experience
• The incumbent may supervise external vendors or partners to execute these activities
• Maintain awareness of new scientific and methodological developments within therapeutic area
• Present outcomes research data at national and international congresses and publish articles in scientific journals.
Research Analyst, Development - Remote
By Memorial Sloan Kettering Cancer Center At New York, NY, United States
At least two years’ experience in prospect development or fundraising.
Strong communications skills, both written and verbal.
Experience evaluating information to make recommendations in a work environment.
Experience with corporations & foundations, healthcare, and/or international philanthropy (a plus).
A good decision-maker, with shown success at making timely decisions.
Able to hold yourself and others accountable to achieve goals and live up to commitments.
Clinical Research Quality Control Associate
By Clinilabs inc At , New York, 10019, Ny $22 an hour
Provide support (e.g. data entry, filing, QC, etc…) to CRU personnel and other Clinilabs personnel ad requested and needed.
Manage and track project timelines and quality issues.
Must have related experience for at least two years.
Must possess excellent clerical, strong computer and good interpersonal skills.
Reading and understanding study protocols.
Communicate with all operational departments regarding project status/issues.
Clinical Research Associate I
By State University of New York Upstate Medical University At Syracuse, NY, United States

Job Summary: Position is Project Manager for a large multi-site clinical trial where Clinical Site is also Coordination Center for the clinical trial. Coordinate all aspects of the clinical trial at ...

Clinical Research Associate Jobs
By Jobot At Brooklyn, NY, United States
Strong organizational and time-management skills.
Collaborate with cross-functional teams to ensure the successful execution of clinical trials, including data management, biostatistics, and medical writing.
Perform site qualification, initiation, and close-out visits, including site selection, site initiation, and site closure.
Identify and escalate study issues to the appropriate stakeholders, including the clinical project manager, medical monitor, and regulatory affairs.
Minimum of 2 years of experience as a CRA in the biotechnology or pharmaceutical industry or academic space
Experience in oncology and solid tumors is required.
Clinical Research Associate Jobs
By Barrington James At New York, United States
MUST have 5+ years experience as a CRA monitoring experience.
MUST have therapeutic experience in Medical Devices or Neurology.
Excellent verbal and written communications skills.
Identify patients eligible for studies
You will ensure monitoring visits are being conducted as needed and tasks are being completed in an appropriate and timely manner
Analyze and prepare data, writing reports and assisting in drafting manuscripts and papers
Clinical Research Associate 2/3-Biotech Solutions - Icon Clinical Research
By Jobs in New York State At Albany, NY, United States

Knowledge of ICH and local regulatory authority regulations regarding drug trials

Clinical Research Monitor, (Remote, Northeast Region), Transcatheter Mitral & Tricuspid Therapies (Tmtt)
By Edwards Lifesciences At New York, NY, 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

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