Senior Clinical Programmer

Company
Cytel
Location
Geneva, Switzerland
Salary
Competitive
Posted
28 Sep 2017
Closes
04 Feb 2019
Ref
CB/SASP/PBS/001

Summary of Job Responsibilities:


As member of the Biostatistics and Data Management (BDM) department, and reporting to the Global Head of Clinical Data Management or to the local manager (Director or Associate Director of Data Management), the main responsibilities of the Clinical Programmer will be to:

Provide for clinical project support across multiple therapeutic areas.

Work closely with data management to ensure data quality.

Contribute to EDC programming and reporting activities.

Work as part of a clinical team developing SAS templates and utilities for data cleaning and reporting;

Able to communicate with all levels of internal team members and sponsors.

Perform quality control measures on deliverables.

Understand and support clinical data management needs. 

Lead clinical programming activities on BDM projects:

Programming (or write validation programs for) and document SDTM deliverables for SDTM Migration;

Developing program specifications and design documents;

being accountable for the quality, traceability, reproducibility and timeliness of programming deliverables,

being accountable for overall client satisfaction with these deliverables,

efficiently communicating with internal and external clients

Ensure the clinical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance:

Clinical study reporting, e.g. ICH E3

Electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation - Part 11

Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM standards

Understand and follow all BDM SOPs as well as any other relevant SOPs.

Keep abreast of current and new programming techniques and other applicable technical advancements while assisting in their implementation

  
Qualifications and Experience:

Minimum Education:

A BA or BS degree or equivalent in computer science, mathematics, statistical or life sciences field. Previous clinical data management or clinical programming experience may substitute for the post-secondary educational requirements.
 

Minimum Work Requirements:

A minimum of 6 years hands on relevant experience in the biotechnology or pharmaceutical industry in clinical development.

Excellent knowledge of SAS SAS BASE, MACRO.

Good Knowledge of CDISC CDASH and SDTM guidelines.

Experience as a lead programmer with and ability to contribute to implementing CDISC models.

Skilled in use of computer technology, including clinical trial databases and applications (e.g., Merge eClinicalOS, Medidata Rave) and ability to learn new applications.

Good Overall understanding of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research

 
 Skills:

Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.

Fluent in English (French and/or German is a plus)

Ability to work effectively in international teams, excellent team player

Ability to work independently is required


 
Compensation & Benefits
We offer a competitive salary-based package and bonus, comprehensive medical, plus a contributing pension plan.
 
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

Cytel does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Cytel’s human resources department to obtain prior written authorization before referring any candidates to Cytel. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Cytel. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Cytel. Cytel shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies.

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