Thermo Fisher Scientific
Sr. Statistical Programmer - FSP - US West Coast Only
Thermo Fisher Scientific, Carlsbad, California, United States, 92002
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We are seeking a full-time Sr. Statistical Programmer
for our client.
* Location:
West Coast based required.
Relocation assistance is NOT provided.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
Discover Impactful Work:
Provides advanced programming support and leads complex data analysis projects. Develops and validates complex statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies.
A day in the Life:
Develop and validate complex statistical programs
Conduct quality control checks on data and analysis outputs
Optimize programming processes and methodologies
Lead complex data analysis projects
Performs quality control checks of SAS code and output produced by other statistical programmers
Codes SAS program for applications designed to analyze and report clinical trial data and for electronic review, transformation, and submission of data in CDISC SDTM format
Document programming activities and maintain version control
Provide technical guidance and support to junior programmers
Ensure compliance with regulatory requirements and industry standards
Review statistical analysis plans and other related documents
Troubleshoot and resolve programming issues
Keys to Success:
Education:
Bachelor's degree in statistics, biostatistics, computer science, or related field
Experience:
4 years+ of experience in statistical programming; proficiency in SAS, R, or Python
Preferred Qualifications:
Experience in clinical trials or research studies; knowledge of CDISC standards (SDTM, ADaM)
Knowledge, Skills, Abilities
Strong analytical and problem-solving skills
Excellent attention to detail and accuracy
Effective communication and interpersonal skills
Ability to lead and mentor junior programmers
Proficiency in Microsoft Office suite
Physical Requirements
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
Performing the responsibilities of the job requires ability to use hands and fingers to handle or feel and to manipulate keys on a keyboard
Occasionally required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.
Ability to read and type while sitting in front of a computer up to 4 hours at a time.
Vision abilities required by the job include close vision
May occasionally have to lift, tug and pull up to 25 lbs.
Compensation and Benefits
The salary pay range estimated for this position Trial Programmer Specialist III based inCalifornia is $104,000.00-$145,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We are seeking a full-time Sr. Statistical Programmer
for our client.
* Location:
West Coast based required.
Relocation assistance is NOT provided.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
Discover Impactful Work:
Provides advanced programming support and leads complex data analysis projects. Develops and validates complex statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies.
A day in the Life:
Develop and validate complex statistical programs
Conduct quality control checks on data and analysis outputs
Optimize programming processes and methodologies
Lead complex data analysis projects
Performs quality control checks of SAS code and output produced by other statistical programmers
Codes SAS program for applications designed to analyze and report clinical trial data and for electronic review, transformation, and submission of data in CDISC SDTM format
Document programming activities and maintain version control
Provide technical guidance and support to junior programmers
Ensure compliance with regulatory requirements and industry standards
Review statistical analysis plans and other related documents
Troubleshoot and resolve programming issues
Keys to Success:
Education:
Bachelor's degree in statistics, biostatistics, computer science, or related field
Experience:
4 years+ of experience in statistical programming; proficiency in SAS, R, or Python
Preferred Qualifications:
Experience in clinical trials or research studies; knowledge of CDISC standards (SDTM, ADaM)
Knowledge, Skills, Abilities
Strong analytical and problem-solving skills
Excellent attention to detail and accuracy
Effective communication and interpersonal skills
Ability to lead and mentor junior programmers
Proficiency in Microsoft Office suite
Physical Requirements
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
Performing the responsibilities of the job requires ability to use hands and fingers to handle or feel and to manipulate keys on a keyboard
Occasionally required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.
Ability to read and type while sitting in front of a computer up to 4 hours at a time.
Vision abilities required by the job include close vision
May occasionally have to lift, tug and pull up to 25 lbs.
Compensation and Benefits
The salary pay range estimated for this position Trial Programmer Specialist III based inCalifornia is $104,000.00-$145,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.