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Clinical Trial Monitor Jobs in Arkansas

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 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 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
Clinical Trial Supply Chain Specialist
By Mindlance At United States
SAP software based computer systems experience.
MS Office and MS Teams experience.
SKYPE Meeting or Virtual Meeting software experience.
GMP and Pharmaceutical Industry Regulations knowledge.
Ability to learn multiple computer systems.
Clinical Trial Liaison Jobs
By Mirum Pharmaceuticals, Inc. At United States
Clinical site management experience, with an understanding of the operational aspects of clinical research and clinical development outsourcing
Excellent written and verbal communication skills - able to interact with all levels of internal and external management
Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning
Other tactical or strategic requirements in line with the study team
5 years’ experience in clinical research in Pharma, Biotech or CRO or related experience
Demonstrated experience of working directly with clinical sites and investigators
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
By EG Life Sciences At United States
5+ years of Global Pharmaceutical Clinical Study Management:
1) 10+ years of Clinical Research Experience:
Audit & Inspection Readiness Experience:
ADDITIONAL QUALIFICATIONS / NICE TO HAVES
1) GCP and Clinical Quality experience
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
Clinical Research Monitor (Remote, Southwest Region) Tmtt
By Edwards Lifesciences At Pueblo-Cañon City 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 Coordinator - Monitoring (Remote)
By Merck At United States
Effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable)
Ensure proper provisioning for Learning Management System (CLMS) for all study site staff.
Credit Management within Learning Management System
Excellent negotiation skills for CTCs in finance area
Clinical Trial Specialist Jobs
By Hawthorne Effect, Inc. At United States
Strong organization skills with experience with balancing priorities and resources.
Visit Management: Support logistics and visit scheduling teams by communicating relevant study information to Clinical Success team
Clinical Trial Experience is highly preferred but not required.
Strong skills in the use of technology, tools, operating systems, and software and is comfortable using these daily.
A creative and resourceful problem-solver with strong critical thinking skills.
GCP and good documentation practice expertise is required
Clinical Trial Assistant / Trial Documentation (Tmf)
By Apex Systems At United States
1. Provide start-up and ongoing trial regulatory document management
5. Setup and manage regulatory document trackers/reports as assigned.
6. Maintain a professional approach respecting the dignity and confidentiality of associates, manager, and vendors.
11. Maintain CEUs for SOCRA or ACRP certification.
• Oncology experience preferred. Prior experience managing flow of clinical trial regulatory documents preferred
4. Ensure quality product deliverables at all times.
Clinical Trial Lead Jobs
By Avania At United States
Ability to work concurrently on multiple protocols and procedures; organizational, time management skills and problem-solving abilities
RN or BA/BS degree in a science/life science, engineering or health-related field plus a minimum 4 years monitoring experience
Experience as mentor and trainer for new CRAs
Excellent communication skills; demonstrated professional writing proficiency
Experience generating project-specific training presentations and coordinating necessary training
Ability to generate monitoring tools; experience generating and giving professional presentations

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?