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Job Details

Centralized Monitoring Analyst (multiple roles)

Company: Docs Global (Continental Europe)
Location: warszawa,Poland
Reference: Ref AS-025786
Closing Date: 15 Aug 18
Type: Permanent
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

DOCS is supporting highly prestigious and one of the world’s top pharmaceutical company that is bringing innovative ideas, products and services continuously improving people’s health. This is a fantastic opportunity for an experienced clinical research professional that is ready to take on a new challenge, further develop their career and enjoy working culture in vibrant Client's office in Warsaw.

Requirements:

Roles & Responsibilities of the position

As a Centralized Monitoring Analyst you will be assessing the logical correctness of the monitoring action requests delivered to study monitors, study level information delivered to the study team and other information recipients. You will also provide ad-hoc report creation and data analysis throughout the studies. You will ensure that risk indicators are correctly set in centralized monitoring systems.


Responsibilities:

- Set-up of the centralized monitoring system (cross-study reporting to Clinical Operations Leadership, Study level reporting to Project Teams, - - Monitoring action requests and alerts)
- Maintenance of the study-specific centralized monitoring system including regular checks of logical correctness of reports and actions requests,
- Communication with monitors and report recipients including training sessions and troubleshooting, follow-up of execution of assigned actions
- Creation of ad-hoc reports including interpretation and translation of user requests into technical considerations

Job Requirements

-Very good spoken and written English
- Previous experience in clinical research (clinical operations technology and standards, Clinical Data Management, Monitoring practices and regulations)
- Programming skills (R or SAS or VBA)
- Solid knowledge of Risk-Based Monitoring (RBM) methodology and tools, industry trends, and role and place of CDM within RBM
- Previous experience from risk based monitoring and centralized monitoring is an advantage
- Scientific background is advantage, BSc Degree or equivalent in the life sciences , technology or related discipline

Remuneration & other details

What is offered
We offer:
· Office based work, no travelling
· Work in the unique organization in Poland with global R&D clinical team
· development opportunities with rapid growing organization


To Apply:
Please contact Dariusz Sternlicht, Recruitment Consultant at DOCS on +48 606 130 397 or email your up-to-date CV to: dariusz.sternlicht@docsglobal.com

About DOCS:
DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical trial industry.

Key words:
Clinical Research Associate, Analyst, Remote Monitor, InhouseCRA, Study Conduct, Regulatory, Pharmaceutical, Risk Based Monitoring, centralized Monitoring, CRO, Pharma, Contract Research Organisation, Biotech, Medical Device, Health, Biotechnology, Chemistry, Permanent, Warsaw, Poland

Apply for this job: Centralized Monitoring Analyst (multiple roles)

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

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