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Clinical Trial Monitor Jobs in New York

Clinical Trial Nurse Navigator
By The Leukemia & Lymphoma Society At Rye Brook, NY, United States
Use problem solving skills to help patients overcome obstacles to enrollment
Maintain/increase knowledge and understanding of hematologic cancers, blood and bone marrow transplant and psychosocial aspects of living with cancer
Outstanding critical thinking, problem-solving, and collaboration skills
Demonstrated commitment to independent learning and skill enhancement
Serve in consulting role to the Information Resource Center about clinical trials
Contribute to continual process improvement of clinical trial support procedures
Clinical Trial Nurse - Nyc, Ny
By IQVIA At , New York $67,000 - $83,200 a year
2+ years of peds experience
Recent experience in drawing blood
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
Director, Clinical Trial Recruitment
By Spectrum Science - a GHMC Company At New York City Metropolitan Area, United States
Meets deadlines, manages priorities and effectively communicates to team members, vendor partners and supervisors.
At least 5-7 years of clinical trial patient recruitment and retention experience working in a global clinical trial environment
Advanced knowledge of Microsoft Office (Outlook, PowerPoint, Word, etc.)
Excellent written and verbal communication skills; strong presentation skills
If you choose to go into an office, take advantage of the pre-tax transportation benefits.
If you choose to work from home, use the office equipment stipend.
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 an exciting opportunity to join a dynamic team of Clinical Trial Monitors? We are looking for a highly motivated individual to join our team and help ensure the success of our clinical trials. As a Clinical Trial Monitor, you will be responsible for overseeing the progress of clinical trials, ensuring compliance with regulatory requirements, and providing support to the clinical team. If you are passionate about clinical research and have a keen eye for detail, this could be the perfect job for you!

A Clinical Trial Monitor is a professional responsible for overseeing the progress of clinical trials. They ensure that the trial is conducted in accordance with the protocol and applicable regulations, and that the safety of the participants is maintained. Clinical Trial Monitors are also responsible for collecting and reporting data, and for providing feedback to the sponsor and investigators. To become a Clinical Trial Monitor, one must have a degree in a relevant field such as medicine, nursing, or life sciences, as well as experience in clinical research. Additionally, Clinical Trial Monitors must possess strong organizational, communication, and problem-solving skills.

Skills required for a Clinical Trial Monitor include:

• Knowledge of clinical trial protocols and regulations
• Excellent organizational and communication skills
• Ability to analyze and interpret data
• Ability to work independently and as part of a team
• Ability to manage multiple tasks simultaneously
• Proficiency in computer applications such as Microsoft Office

Knowledge required for a Clinical Trial Monitor includes:

• Clinical research processes
• Good Clinical Practice (GCP)
• Clinical trial regulations
• Data collection and analysis
• Quality assurance and control

Responsibilities of a Clinical Trial Monitor include:

• Reviewing and approving study protocols
• Ensuring that the trial is conducted in accordance with the protocol and applicable regulations
• Monitoring the progress of the trial and providing feedback to the sponsor and investigators
• Collecting and reporting data
• Ensuring the safety of the participants
• Ensuring that the trial is conducted in an ethical manner
• Maintaining accurate records

Experience required for a Clinical Trial Monitor includes:

• Previous experience in clinical research
• Previous experience in a related field such as medicine, nursing, or life sciences
• Previous experience in data collection and analysis

Qualifications required for a Clinical Trial Monitor include:

• Bachelor’s degree in a relevant field such as medicine, nursing, or life sciences
• Certification in Good Clinical Practice (GCP)
• Knowledge of clinical trial protocols and regulations

Tools that help Clinical Trial Monitors work better include:

• Clinical trial management systems
• Electronic data capture systems
• Quality assurance and control systems
• Data analysis software

Good tips to help Clinical Trial Monitors do more effectively include:

• Stay up to date on clinical trial regulations and protocols
• Develop strong organizational and communication skills
• Develop problem-solving skills
• Develop an understanding of data collection and analysis
• Develop an understanding of quality assurance and control

Common Clinical Trial Monitor interview questions include:

• What experience do you have in clinical research?
• What is your understanding of clinical trial protocols and regulations?
• How would you ensure the safety of the participants in a clinical trial?
• How would you ensure the accuracy of data collection and reporting?
• What experience do you have in data analysis?