Register
Recruit Create CV

Clinical Trial Monitor Jobs

Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
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 Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
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
Associate Clinical Research Monitor (Remote) Thv
By Edwards Lifesciences At , $64,000 - $91,000 a year
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Good problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Technical writing skills (protocols, CRF development, study tools)
Good computer skills in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery
Experience with electronic data capture preferred
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
Clinical Trial Assistant Jobs
By RemeGen Biosciences At Pennsylvania, United States
Assist with general response to patient enrollment inquiries and seek management support when needed.
Manage SVP and study team calendars and set up meetings.
Excellent written and verbal communication skills.
Strong attention to detail and problem-solving skills.
· 3+ years of experience in health care, biopharmaceutical experience is strongly preferred.
Assist the clinical development teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Coverage Analyst, Remote
By University of Maryland Medical System At Baltimore, MD, United States
Skill in cost/financial accounting and clinical trial management software.
IV. Knowledge, Skills, And Abilities
Bachelor’s degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field required.
Certification in Healthcare Research Compliance or Epic preferred.
Demonstrated skill tracking clinical and corporate contracts using electronic administration software such as Grant.gov, CICERO, OnCore, Epic, etc.
Creates coverage analysis grids and analyzes the performance of the actual coverage analysis.
Clinical Research Monitor (Remote) Tmtt
By Edwards Lifesciences At Albuquerque-Santa Fe Metropolitan Area, 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
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 Trial Intern - Dallas, Tx
By Medpace, Inc. At , Irving, 75038, Tx
Excellent organizational, communication, and prioritization skills;
Knowledge of Microsoft Office; and
Competitive compensation and benefits package
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
Perform administrative duties in conformity with company policies and procedures;
Clinical Trial Research Assistant
By Durham Technical Community College At , , Nc $48,000 a year

% High School diploma or equivalent

Clinical Trial Coordinator (Cqm) - Home-Based
By ICON At , Remote
B.S. or Advanced Degree (or equivalent degree/experience in the opinion of the Hiring Manager)
Manages the collection and retention of training signature logs
Minimum of 1-4 years of relevant work experience
Strong communication (written and verbal) skills to be able to interact with internal Vertex groups as well as external groups
Demonstrates a working knowledge of ICH GCP regulations and clinical protocols
Distributes SUSAR reports to investigators
Early Clinical Development Monitor
By Parexel At , Remote
Performs site management activities to ensure compliance to the protocol, monitoring plan, GCP, ICH, applicable federal/local regulations, and SOPs
Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements
Conducts site qualification, initiation, interim, and close-out visits
Performs drug accountability, reconciliation, and destruction. Verifies storage and shipment requirements are according to protocol
Travels to clinical study sites as required, including remote or onsite visits globally
Analytical problem-solving experience, trouble shooting and resourcefulness
Clinical Trial Analyst Jobs
By Randstad Life Sciences US At Cambridge, MA, United States
Supporting additional ad-hoc activities as needed, as agreed with CTA Manager.
Maintaining knowledge of systems and processes.
Perform departmental tasks as needed.
Review and/or approval of study documentation, including essential document packets, study plans, informed consent forms, etc.
Supporting oversight of risk-based monitoring.
Attendance of key team meetings as required; may make presentations (e.g. data, etc.).
Clinical Research Monitor (Remote, Midwest/Northeast Region) Tmtt
By Edwards Lifesciences At Greater Owensboro Area, 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
Clinical Trial Assistant / Etmf (Electronic Trial Master File) Coordinator
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Knowledge of clinical research processes, regulatory requirements, and good clinical practice (GCP).
Familiarity with eTMF systems and other clinical trial management systems.
Liaise with project managers, clinical operations staff, and other relevant team members to facilitate document collection and retention.
Monitor the progress of clinical trials and report updates to the project manager or clinical team lead.
Previous experience in a similar role, preferably within a pharmaceutical or biotech environment.
Excellent organizational skills and attention to detail.
Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities
100% Remote- Clinical Trial Educator
By Actalent At Parsippany, NJ, United States
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Seeking 1 Clinical Trial Educator
PART TIME ROLE- 20hrs a week avg.
DE&I Are Embedded Into Our Culture Through

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?