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Clinical Trial Monitor Jobs

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 Trial Educator Jobs
By Actalent At Westerville, OH, United States

Description The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The ...

Clinical Trial Educator Jobs
By Actalent At West Palm Beach, FL, United States

Description The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The ...

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
Remote Clinical Trial Project Coordinator
By Confidential At Durham, NC, United States
Coordinates a multitude of CTM tactical and project management activities throughout the clinical trial lifecycle including forecasting/planning.
Management/tracking of global drug shipments; and Investigational Medicinal Product (IMP) accountability/ disposition.
NOTE: Can be fully remote but must be willing to come onsite the first 2 weeks for training.
Contract position: 1 year to start with potential for extension or conversion.
Note: 30-40 hours per week.
Implementation/oversight of IVRS/IWRS systems for drug supply.
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 Assistant - Milan
By DOCS At All, MO, United States

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, ...

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 Assistant Jobs
By Precirix At Greater Boston, United States
·Expected educational qualifications: BSc or equivalent
·Minimum 2 years’ experience in with a clinical trial related role
·Experience with digital clinical trial systems such as eTMF, EDC, IRT etc
·Excellent communication skills (verbal, written and interpersonal) and negotiation skills
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Clinical Trial Assistant, Langen Hybrid
By DOCS At All, MO, United States
If you have a completed education in any ad
medical device and government and public health
ife science area (hotel, business a
Clinical Trial Administrator-1 Jobs
By PharmiWeb.Jobs: Global Life Science Jobs At South Carolina, United States
Note - Specific skills and experience requirements may vary depending on the Country
Performs data entry into various databases/applications
Manages meetings/logistics, payments, and document archives
Undergraduate degree or relevant experience - at the discretion of the CRD
1 year experience in relevant administration (depending on the tasks required).
Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt
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 Jobs
By DOCS At All, MO, United States
Previous administrative experience preferably in the medical/ life science field.
Proven organizational and administrative skills.
Good knowledge of spoken and written Dutch and English.
• Contributes to the production and maintenance of study documents, en
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.
Ycci Clinical Research Associate (Monitor)
By Yale University At , New Haven, 06519, Ct
Preferred Education, Experience and Skills:
SOCRA/ACRP (or equivalent) certification; Master’s Degree or other advanced degree in related field.
YCCI Clinical Research Associate (Monitor)
None - Not included in the union (Yale Union Group)
Click here to see our Wage Ranges
Total # of hours to be worked:
Clinical Trial Administrator Ii
By PSI CRO AG At Durham, NC, United States
Be responsible for document management
College/University degree or an equivalent combination of education, training & experience
Administrative work experience, preferably in an international setting
Prior experience in Clinical Research
Be the point of contact for investigational sites, vendors, and multi-functional project teams
Update and maintain (automated) tracking systems and schedules
Clinical Trial Educator Jobs
By IQVIA At , Remote
Some roles require direct interaction with patients to offer education on trial, disease, and/or device/medication
Provides education to health care professionals and their staff, reinforces study protocols as related to a clinical trial
Maintains up-to-date technical knowledge of specialty and disease areas
Bachelor's Degree BA/BS in Health Sciences or related field or equivalent academic professional qualifications. Req
Typically requires 1 - 2 years of prior relevant experience. Req
Excellent interpersonal and communication skills
Clinical Trial Educator – Pediatric Cardiology – Nationwide – Hab80850
By IQVIA At , Remote
Some roles require direct interaction with patients to offer education on trial, disease, and/or device/medication
Provides education to health care professionals and their staff, reinforces study protocols as related to a clinical trial
Maintains up-to-date technical knowledge of specialty and disease areas
Bachelor's Degree BA/BS in Health Sciences or related field or equivalent academic professional qualifications. Req
Clinical Research Experience. 2 yrs Req
Excellent interpersonal and communication skills

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?