Senior Statistical Programmer, Accra, IQVIA

Senior Statistical Programmer, Accra, IQVIA

Role Responsibilities/ Responsabilités du rôle

Senior Statistical Programmer


Primary Location: Aschheim, Bavaria, Germany

Additonal Locations: Accra, Ghana,GHA; Amsterdam, Netherlands,NLD; Antwerp, Belgium,BEL; Barcelona, Spain,ESP; Beirut, Lebanon,LBN; Belville, South Africa,ZAF; Bucharest, Romania,ROU; Budapest, Hungary,HUN; Budapest, Hungary,HUN; Cheraga, Algeria,DZA; Copenhagen, Denmark,DNK; Espoo, Finland,FIN; Kaunas, Lithuania,LTU; Kiev, Ukraine,UKR; Lagos, Nigeria,NGA; Madrid, Spain,ESP; Moscow, Russia,RUS; New Cairo, Egypt,EGY; Oslo, Norway,NOR; Sarajevo, Bosnia,BIH; Sofia, Bulgaria,BGR; Tallinn, Estonia,EST; Tunis, Tunisia,TUN; Vienna, Austria,AUT; Warsaw, Poland,POL; Zaventem, Belgium,BEL

Full time



Senior Statistical Programmer:

Job Family Description

Conducts statistical analyses for client reports and publications, performs advanced statistical programming and biostatistical analyses and utilizes findings, and insights for practical application to further business operations, come across innovative findings and discoveries for solution and product development.

Sub-Family  Description

Develops, executes, and reviews programs to provide statistical programming support for statisticians, clients, or business demands to source, organize (creating statistical tables, listings, and graphs) and interpret complex data sets.

Creates programming specifications, program development, program validation, and program output finalization associated with analysis datasets, tables, figures, listings, and regulatory submission data packages; and provides programming support for additional business needs such as safety reporting, patient data reviews, and risk mitigation.

Job Details:

Position: – Sr. Statistical Programmer

Home Based (mostly)

Min 3+ years of CRO/Pharma Industry

Therapeutic Areas: Oncology // Immunology // IDV // EDCP

Key Skills:

Preferred to have R programming

Must have SAS® Base, and good knowledge of SAS® graph and SAS® Macros.

Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician.

Must have excellent knowledge of CDISC standards (SDTM and ADaM)

Thorough understanding of relational database components and theory.

Excellent application development skills.

Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.

Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes.

Minimum of 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industry

Good verbal and written communication skills.

Ability to work on multiple projects, plan, organize and prioritize activities.

Required Knowledge, Skills and Abilities:

Experience as technical team lead directly engaging clients and coordinating tasks within a programming team

In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Knowledge of statistics, programming and/or clinical drug development process

Advanced knowledge of R programming

Base SAS, SAS/STAT, SAS Graph and SAS Macro Language

Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.


Good organizational, interpersonal, leadership and communication skills

Ability to independently manage multiple tasks and projects

Ability to delegate work to other members of the SP team

Excellent accuracy and attention to detail

Ability to delegate work to other members of the SP team [SPM]

Exhibits routine and occasionally complex problem-solving skills

Ability to lead teams and projects and capable of managing at a group level

Recognizes when negotiating skills are needed and seeks assistance.

Ability to establish and maintain effective working relationships with co-workers, managers and clients.


Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files  for internal and external clients and (iii) the programming  quality control checks for the source data and report the data issues periodically..

Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.

Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.

Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.

Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.

Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

Use and promote the use of established standards, SOP and best practices.

Provide training and mentoring to SP team members and Statistical Programming department staff.


Bachelor’s degree from reputable university preferably in science/ mathematics related fields

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at

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