Sr SAS Programmer
Company Name:
ICON plc
Senior Statistical Programmer
Location - Local to Baltimore office preferred, will consider telecommute for the right candidate.
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development
services
to the pharmaceutical, biotechnology and medical device industries.
Overview of the Role
Responsible for leading projects.
Responsible for performing programming activities according to business SOPs and sponsor requirements.
Responsible for providing accuracy of results and providing appropriate documentation.
Responsible for generation of documentation and SAS code required and generation of report tables and listings.
Responsible for planning software specifications and data structures for studies.
Responsible for review of database set-up, data import and acceptance testing if required.
Responsible for participation in study database design and set up activities ensuring that the needed systems specifications are appropriate and complete.
Give feedback to support continuous improvement of programming activities.
To work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
Travel (approximately 5%) domestic and/or international.
Act as study lead for a project to coordinate all study activities and provide input to project documentation as appropriate including review statistical analysis plans and CRF's.
Ensure projects are conducted in accordance with internal SOPs, client requirements, and Good Clinical Practices (GCP).
Carry out quality control checks to ensure compliance with Company and Sponsor requirements.
Ensure accuracy of all results and ensure appropriate documentation.
Prepare graphs, tables and listings for inclusion in clinical study reports.
Write/follow appropriate SOPs and WPS for programming activities.
Provide mentorship and training for other programmers.
Provide support to the Principal Statistical Programmer and
manager
, Statistical Programming.
Ensure compliance with all training requirements.
Provide data transfers to company or sponsor standards.
Attend and present at external meetings as appropriate.
Under supervision perform senior review of complete programming deliverables.
Participate in client audits where appropriate.
Liaise with Data Management, QA, PK, Medical Writing, Stats and PM.
Role Requirements / Skills / Experience Required
Bachelor's degree or local equivalent within a mathematical or computing or life sciences discipline is preferred.
Preferably 5 year's previous experience within a similar role including relevant experience of leading projects.
Problem solving skills.
Attention to detail.
Good verbal and written communication skills.
Preferably an awareness of CDISC standards, regulatory requirements and industry best practice.
Due to the nature of this
position
it may be required for the
employee
to travel. Therefore, dependent on the employee's location, the employee may be required to possess a valid driver's license.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
In addition you will have the opportunity to develop within your role and take on further responsibilities or develop your skill set within other related departments of ICON.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Please send me a updated copy of your resume for further review. If not interested please forward my details to someone in your network who might be interested.
Thanks in advance.
Warmest Regards,
Nishi Joshi
Talent Acquisition Sourcing Specialist
ICON Clinical Research
2100 Pennbrook Parkway, North Wales PA 19454
Email:
Web: www.iconplc.com
Estimated Salary: $20 to $28 per hour based on qualifications.
ICON plc
Senior Statistical Programmer
Location - Local to Baltimore office preferred, will consider telecommute for the right candidate.
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development
services
to the pharmaceutical, biotechnology and medical device industries.
Overview of the Role
Responsible for leading projects.
Responsible for performing programming activities according to business SOPs and sponsor requirements.
Responsible for providing accuracy of results and providing appropriate documentation.
Responsible for generation of documentation and SAS code required and generation of report tables and listings.
Responsible for planning software specifications and data structures for studies.
Responsible for review of database set-up, data import and acceptance testing if required.
Responsible for participation in study database design and set up activities ensuring that the needed systems specifications are appropriate and complete.
Give feedback to support continuous improvement of programming activities.
To work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
Travel (approximately 5%) domestic and/or international.
Act as study lead for a project to coordinate all study activities and provide input to project documentation as appropriate including review statistical analysis plans and CRF's.
Ensure projects are conducted in accordance with internal SOPs, client requirements, and Good Clinical Practices (GCP).
Carry out quality control checks to ensure compliance with Company and Sponsor requirements.
Ensure accuracy of all results and ensure appropriate documentation.
Prepare graphs, tables and listings for inclusion in clinical study reports.
Write/follow appropriate SOPs and WPS for programming activities.
Provide mentorship and training for other programmers.
Provide support to the Principal Statistical Programmer and
manager
, Statistical Programming.
Ensure compliance with all training requirements.
Provide data transfers to company or sponsor standards.
Attend and present at external meetings as appropriate.
Under supervision perform senior review of complete programming deliverables.
Participate in client audits where appropriate.
Liaise with Data Management, QA, PK, Medical Writing, Stats and PM.
Role Requirements / Skills / Experience Required
Bachelor's degree or local equivalent within a mathematical or computing or life sciences discipline is preferred.
Preferably 5 year's previous experience within a similar role including relevant experience of leading projects.
Problem solving skills.
Attention to detail.
Good verbal and written communication skills.
Preferably an awareness of CDISC standards, regulatory requirements and industry best practice.
Due to the nature of this
position
it may be required for the
employee
to travel. Therefore, dependent on the employee's location, the employee may be required to possess a valid driver's license.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
In addition you will have the opportunity to develop within your role and take on further responsibilities or develop your skill set within other related departments of ICON.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Please send me a updated copy of your resume for further review. If not interested please forward my details to someone in your network who might be interested.
Thanks in advance.
Warmest Regards,
Nishi Joshi
Talent Acquisition Sourcing Specialist
ICON Clinical Research
2100 Pennbrook Parkway, North Wales PA 19454
Email:
Web: www.iconplc.com
Estimated Salary: $20 to $28 per hour based on qualifications.
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