Associate RTSM Specialist Job at Worldwide Clinical Trials - USA, Research Triangle Park, NC

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  • Worldwide Clinical Trials - USA
  • Research Triangle Park, NC

Job Description

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 over 3,500+ 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.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

SUMMARY: To coordinate and perform processes associated with the configuration, maintenance, and validation of databases and database systems and associated applications.

RESPONSIBILITIES:

Tasks may include but are not limited to:


  • To liaise with relevant staff to determine the allocation of tasks, to establish timelines, to report progress and any issues outstanding.
  • To assist in the review of specifications for the set-up and modification of project specific data entry software (including edit check specifications).
  • To assist in the review of the validation plan for edit check and reconciliation check specifications.
  • Under supervision of the CDP, develop, test and run SAS programs for clinical data management. This includes programs for data validation and reconciliation checks, data listings and data transfers.
  • Under supervision of the CDP,configure database/eDC software (both internal and 3rdparty) for the use of DM, sponsor and sites.
  • To perform testing of databases and related applications according to IT and Data Management departmental SOPs, both for initial set-up and maintenance.
  • Under supervision of the CDP, run database upload programs and to process any error reports.

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

OTHER SKILLS AND ABILITIES:
  • Be able to demonstrate good written and verbal communication skills.
  • Be able to demonstrate a methodical and logical approach to problem solving and the ability to learn new tasks quickly.
  • Be able to work with close attention to detail.
  • Be questioning about the validity of data being entered/extracted.
  • Be hardworking and efficient.
  • Possess good team working skills.
  • Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
  • The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.

REQUIREMENTS:
  • Be educated to degree levelor relevant experience
  • At least 2 years plus experience of Data Management Systems and Software
  • An understanding of CDISC SDTM standards

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit or connect with us on LinkedIn .

Job Tags

Permanent employment, Worldwide,

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