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Clinical Trial Monitor Jobs in Pennsylvania

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 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.
Comparator Sourcing Specialist - Clinical Trial Supply
By Eurofins Lancaster Laboratories At Horsham, PA, United States
Good organizational and time management skills
Proven work experience, preferably in a GMP area
Proficiency in Microsoft Word, and experience with ERP preferable
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Acting as primary point of contact internally for comparator sourcing
Advises on appropriate sourcing strategy
Clinical Trial Coordinator Jobs
By BriaCell Therapeutics Corp. At Philadelphia, PA, United States

We seek a clinical trial coordinator who worked at a patient care level, to supervise sites remotely from the Sponsor's perspective.

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?