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Job Details

Sr Analyst, Statistical Programming

Type

Full time

Location
USA-California-Remote
Job reference

Req-39696

Posted for

2 days ago

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.


 

How you’ll make an impact:

·       Plan the execution of programs in statistical programming languages within project.

·       Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations; Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g SAS)

·       Review and validate statistical programs and ensure that all appropriate program validation documentation to meet regulatory and company standards are consistently structured to permit efficient programming, reporting, and review

·       Perform complex analysis in response to data requests in collaboration with designated statistician

·       Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report Forms), database specifications, and perform edit checks
Other duties assigned by Leadership

What you'll need (Required):

Bachelor's Degree in Statistics, Mathematics, Computer Science or related field with 4 years of previous statistical programming experience (e.g. SAS) Required or
Master's Degree or equivalent in Statistics, Mathematics, Computer Science or related field, with 2 years experience previous statistical programming experience (e.g. SAS) Required

What else we look for (Preferred):

·       Proven expertise in interfacing MS Office Suite with SAS

·       Good written and verbal communication skills and interpersonal relationship skills including consultative and relationship management skills

·       Full understanding and knowledge relevant to statistical programming

·       Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting

·       Strong problem-solving, organizational, analytical and critical thinking skills

·       Experience working in clinical trials within a pharmaceutical/medical device industry

·       Good leadership skills and ability to influence change

·       Strict attention to detail

·       Ability to interact professionally with all organizational levels

·       Ability to manage competing priorities in a fast paced environment

·       Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on projects

·       Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations

·       Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

 

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $116,000 to $164,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.   

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Job reference

Req-39696

Apply Now
Type

Full time

Location
USA-California-Remote
Posted for

2 days ago


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Apply Now
About Edwards Lifesciences

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.


Important Notices for Candidates

COVID Vaccination Requirement Notice

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

For US Applicants Only

Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable regulation.

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