Associate / Clinical Database Programmer (Sas)
2 weeks ago
**Requisition Number**7609**
**Employment Type**:Regular**
**Who we are**
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
**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
**What Global Data Management does at Worldwide**
Data Management is an ever growing and collaborative department. Our global team is a group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies beginning with building the study database, to locking and delivering the final dataset for the project. Data Management reviews and ensures the clinical study data is of high quality for regulatory submissions.
The Data Management group is the perfect place to launch or further your career. Whether it is technical expertise, or coming from a clinical background, you’re able to hone and expand your skillset within our department. Spanning various roles from data support staff, database and SAS programmers, coders and functional leads, there is place for you
**What you will do**
- To review specifications for the set-up and modification of project specific data entry software (including edit check specifications). Review validation plan for edit check and reconciliation check specifications.
- Develop, test and run SAS programs for clinical data management. This includes programs for data validation and reconciliation checks, data listings and data transfers.
- To run database upload programs and to process any error reports.
**What you will bring to the role**
- 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.
- Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
**Your experience**
- Be educated to degree level
- Have experience of Data Management Systems and software
- An understanding of CDISC SDTM standards
- Experience of SAS programming language
We love knowing that someone is going to have a better life because of the work we do.
LI-PL1
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Nottingham, United Kingdom Worldwide Clinical Trials Full timeWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...
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