Senior Statistical (SAS) Programmer
Ref: 00382
This is an excellent opportunity for an experienced Statistical Programmer,
preferably with experience in SAS used in clinical trials, to work in a senior role
for one of the global giants in the pharmaceutical world that is known as a
leading name in the discovery, development and marketing of innovative
pharmaceutical products. The role is based at the companys US office in New
Jersey.
JOB ROLE: The Senior Statistical Programmer is responsible for all programming
aspects (analysis datasets, pooled datasets, listings and tables) of individual
Phase I-IV clinical trials and project level activities for small drug
project/indications.
PRINCIPAL RESPONSIBILITIES include:
Leading programming activities for a trial, early phase project,
indication or publication activities.
Lead a complex/large project under supervision of a Programme
Statistician/Group Head.
Maintaining efficient interfaces with internal and external
customers.
Developing resource plans as required with support of the Group
head.
Developing and complying with project/study standards and
specifications.
Providing input into study protocol, CRF and data structures
tables, listings and figures for phase I-IV clinical trials and submission
activities.
Programming, according to specifications, analysis datasets,
pooled datasets, listings, tables, and figures for phase I-IV clinical trials and
for SCS and SCE with high quality and within milestones.
With the statistician, developing specifications for analysis
datasets, pooled datasets and listings.
Supporting quality control and quality audit of deliverables.
Maintaining records for all assigned projects and archiving of
trial/project analysis and associated documentation.
Participating in CRO selection and supervising the SR trial activities
of the CROs.
Providing input on process improvement initiatives and
participating in non-clinical project activities.
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Minimum of a BA/BS or equivalent experience in Mathematics,
Statistics, Computer Science, Life Science or related field(s).
At least 3 years experience in a programming role preferably
supporting clinical trials/or in the pharmaceutical industry (2 years for MS
candidates).
Intermediate knowledge of/experience with SAS software
Working knowledge of database design/structures.
Good understanding of global clinical trial practices, procedures,
methodologies.
Good understanding of regulatory requirements, ICH, GCP
Intermediate knowledge of office tools.
Fluent English (oral and written)
BENEFITS OF THE ROLE: This is one of the worlds top pharmaceutical
companies and known to be dedicated to best practice in leadership, giving
encouragement to innovation and creativity in its employees and offering a
work culture of mutual respect, integrity and loyalty. They have a great
pipeline of products in development guaranteeing excellent career prospects.
Fforde is a uniquely specialised recruitment agency/business for the
pharmaceutical, clinical research and biotechnology sectors. For applications
please email your CV to: [log in to unmask] or speak to our
specialist consultant, Den Lowpetch on +1 212 520 8303 who will be pleased
to give you further information and advice on your personal career needs.
Visit our website and see all our job opportunities at www.fforde-
management.com
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