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Clinical Data Management Associate II

Employer
Worldwide Clinical Trials
Location
Bucharest, Romania
Salary
Competitive
Start date
25 May 2022
Closing date
23 Jun 2022

View more

Discipline
Data Management / Statistics
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What you will do
SUMMARY: The Clinical Data Management Associate II is responsible for overall database design, electronic case report form design, monitoring, management, processing, and archival of clinical data. You will interact with Sponsors and internal staff regarding related data, study timelines, and compliance issues.
  • Designs study database to ensure accurate creation of eSource and case report forms for data collection and reports
  • Performs verification and User Acceptance Testing (UAT) of configured databases and database lock/unlock procedures
  • Reviews study protocol, monitors quality checks, identifies/resolves discrepancies, and tracks timeliness
  • Prepares documents, reports, and assists in corrective actions for findings
  • Manages archival of clinical trial documents (paper and electronic records)
  • Creates guidelines, access instructions, and provides support/training to those using the database

What you will bring to the role
  • Professionalism in behavior and appearance and customer service
  • Excellent written/oral communication skills and ability to understand complex instructions
  • Computer systems and applications knowledge
  • Strong interpersonal skills, attention to detail, organizational skills, and ability to meet deadlines
  • Knowledge of the clinical research process, including Good Clinical Practice

Your experience
  • Bachelor’s degree (preferably in the field of Health)
  • At least 3 years of quality control/quality assurance, and data management of regulatory documents in the clinical research field

    Why Worldwide
    At Worldwide , we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does.Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

    Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!

#LI-SH1
#IND-SH1
#LI-Romania

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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