Dear Allstat, 

 

CK Clinical are recruiting for a Project Statistician to work within the
Oncology therapy area of this leading Pharmaceutical organisation based
in the UK. Interacting with European colleagues across various
locations,  you will be involved in the development of protocol designs,
clinical plans, and data analysis plans in collaboration with
physicians, veterinarians, and/or medical colleagues. You will also be
responsible for working with research associates and scientists to
establish a reporting database and for analysing data for these types of
studies. 

The main responsibilities of the role includes: 

Statistical Trial Design and Analysis 
* Operate in collaboration with study personnel to provide input on
study protocol, design studies and write protocols for the conduct of
each study. 
* Assist in or be accountable for selecting statistical methods for data
analysis, authoring the corresponding sections of the protocol, and
conducting the actual analysis once a reporting database is created. 
* Collaborate with data management in the planning and implementation of
data quality assurance plans. 
* Maintain currency with respect to statistical methodology, to maintain
proficiency in applying new and varied methods, and to be competent in
justifying methods selected. 
* Participate in peer-review work products from other statistical
colleagues. 


Communication of Results and Inferences 
* Collaborate with team members to write reports and communicate
results. 
* Assist with, or be responsible for, communicating study results via
regulatory submissions, manuscripts, or oral presentations in group
settings, as well as for communicating one-on-one with key customers and
presenting at scientific meetings. 
* Respond to regulatory queries and to interact with regulators. 

Therapeutic Area Knowledge 
* Understand disease states in order to enhance the level of customer
focus and collaboration and be seen as a strong scientific contributor. 

Regulatory Compliance 
* Perform work in full compliance with assigned curriculum(s) and will
be responsible for following applicable corporate, medical, local, and
departmental policies, procedures, processes, and training. 

Interested applicant will be qualified to MSc level in Statistics,
Biostatistics, Medical Statistic (OR Equivalent) and will be proficient
in SAS programming. You will have excellent interpersonal communication
skills for effective customer consultation, together with a working
knowledge of experimental design and statistics. Self-management skills
with a focus on results for timely and accurate completion of competing
deliverables is essential together with resource management skills and
proven problem solving ability and strategic thinking. Business process
expertise associated with critical activities (e.g. regulatory
submissions) is also desirable.

 

This is an excellent opportunity for a candidate who is looking to
develop their career within an established Pharmaceutical organisation.
Salary on offer is negotiable and dependant upon experience and can be
discussed upon application.

 

For immediate consideration, please contact Priya Mukherjee on
+44(0)1438 870028 or email an updated CV to [log in to unmask]

 

Best wishes,

 

Priya

Priya Mukherjee BSc (Hons) MRec CertRP

Senior Consultant

 

CK Clinical Limited

9 High Street

Stevenage Old Town

Hertfordshire

SG1 3BG

 

DD: +44 (0)1438 870028

Mobile: +44 (0) 7714 288632

Tel: +44 (0)1438 743047

Fax:+44 (0)1438 723800

 

 

 


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