This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Senior Clinical Programmer

Laboratory Corporation of America Holdings (Covance)

Maidenhead, United Kingdom

Job Overview:

Sr Clinical Programmer Crystal Reports

permanent, salaried

Remote from anywhere in the UK

 

DESCRIPTIONExperience programming reports in Crystal ReportsGenerating reports like RAVE Dictionary Search tool; RAVE Object Search Tool that can be used a reference during study build using Cognos BIProgramming of the custom Business Objects (BO4) reports on the ad-hoc basis for the data validation of the clinical database.Maintains all required study documentation.Support development and review of SOPs, and Work Guidelines to promote consistency.Identify additional opportunities for standardization and departmental efficiency.Preferred: implementation of industry standards CDISC-SDTM/CDASH for a Standard Global Library set-up in Medidata RAVEEducation/Qualifications:

Minimum Required:

• University/college degree (life science, computer science, programming, pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.g., nursing certification, computer science, medical or laboratory technology).

• Broad knowledge of drug development process.

• Basic knowledge of budgets and relationship to productivity targets.

• Working knowledge of CDISC.

• Working knowledge of System Life Cycle in relationship to the implementation new applications.

• Fluent in English, both written and verbal.

 Experience:

Minimum Required:

• Minimum 4 years of relevant work experience to include programming in Crystal reports

• Demonstrate excellent problem solving skills, a proactive approach and the ability to make sound decisions.

• Demonstrated skill in leading teams, by example and mentoring staff.

• Excellent oral and written communication and presentation skills.

• Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC.

• Experience working with Medidata Rave

• Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.

• Demonstrated ability to work in a team environment.

• Demonstrated ability to handle multiple competing priorities.

• Proven managerial and interpersonal skills.

 

 

Job posted: 2020-06-01

3
Subscribe