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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
Clinical Research Associate I (Part-Time)
By Binghamton University At Stony Brook, NY, United States

In accordance with the Title II Crime Awareness and Security Act

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.
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

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Associate to join our team and help us develop and execute clinical studies. You will be responsible for managing clinical trials, ensuring compliance with applicable regulations, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview:

A Clinical Research Associate (CRA) is a healthcare professional who works in clinical research and is responsible for monitoring the progress of clinical trials. The CRA is responsible for ensuring that clinical trials are conducted in accordance with the protocol, applicable regulations, and ethical standards.

Detailed Job Description:

A Clinical Research Associate is responsible for the planning, coordination, and execution of clinical trials. This includes the development of study protocols, the selection of clinical sites, the recruitment of study participants, the collection and analysis of data, and the reporting of results. The CRA is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and ethical standards.

What is Clinical Research Associate Job Skills Required?

• Knowledge of clinical research principles, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Attention to detail and accuracy
• Proficiency in Microsoft Office applications

What is Clinical Research Associate Job Qualifications?

• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Certification as a Clinical Research Associate (CCRA) or Clinical Research Professional (CRCP)

What is Clinical Research Associate Job Knowledge?

• Knowledge of clinical research principles, regulations, and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial design and data analysis

What is Clinical Research Associate Job Experience?

• Previous experience in clinical research or related field
• Experience in monitoring clinical trials
• Experience in data collection and analysis

What is Clinical Research Associate Job Responsibilities?

• Develop and implement clinical trial protocols
• Monitor clinical trial sites to ensure compliance with protocol and applicable regulations
• Recruit and screen study participants
• Collect and analyze data
• Prepare and submit reports to regulatory agencies
• Maintain accurate and up-to-date records
• Ensure the safety of study participants