This listing was posted on Manatal ATS.
Clinical Programmer Principal
Location:
London, Gt Lon
Description:
The Principal Clinical Programmer conducts and coordinates programming activities for multiple studies. As an advanced practitioner in data management programming, provides technical advice and support for programming activities to data management team. May oversee the work product of other programmers, ensuring high quality and timeliness.Experience in Pharma/Biotech is essential. Key Duties and Responsibilities: Excellent understanding of SQL programming concepts and ability to write complex SQL programming code. Ability to configure a study/project using an ETL tool and write complex SQL queries for report development. Ability to ingest data from various data sources and also integrate the data from external applications using the ETL tool. Very high understanding of the Phase I-IV clinical trial process Experience working in the Clinical data management function. Thorough understanding of the DM related study activities like CRFs, reconciliation, Manual data reviews etc. Ability to understand the department level SOPs, WIs Knowledge about GxP systems and regulatory framework of the clinical systems Required to handle the clinical studies in CDSM independently and with minimal supervision. Collaborate with the stakeholders in CDSM (data managers, data review team, recon team) during the study and provide necessary Clinical programming input and provide solutions Ability to keep track of the clinical study milestones and align them with timely delivery of the reports. Ability to understand/speak in a concise and clear manner in all the department/study team level meetings and explain the issue/concerns from the programming point of view. Ability to develop any programming guidelines/documents if necessary. Providing creative programming solutions based on the day-to-day study and DM process challenges. Ability to devise methodical approaches to solve the problems and proactively identify the possible risks/problems. Knowledge and Skills: High proficiency in Programming languages in CDMS like SAS/ETL and SQL Plus and good knowledge of data standards, such as CDISC and SDTM High proficiency in Clinical Data Management procedures including good knowledge of Good Clinical Practices (GCP), 21 CFR part 11 and other regulatory requirements Strong organizational, influencing, presentation, documentation, and interpersonal skills as well as a team-oriented approach. Significant, demonstrated experience with clinical programming, clinical data management, CRO industry and data reporting along with languages such as SAS and SQL. Proven ability to independently determine the most appropriate methods and procedures across Clinical Data Management projects Displays strong writing and verbal presentation skills, ability to convey complex/technical information to a variety of audiences and build alignment around an issue Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.Please use the below Lifelancer link for job application and quicker response. https://lifelancer.com/jobs/view/02cd7e8ee4b5a8b25b387a0cd1259dfe
Company:
Lifelancer
Posted:
August 9 on Manatal ATS
Visit Our Partner Website
This listing was posted on another website. Click here to open: Go to Manatal ATS
Important Safety Tips
- Always meet the employer in person.
- Avoid sharing sensitive personal and financial information.
- Avoid employment offers that require a deposit or investment.
To learn more, visit the Safety Center or click here to report this listing.