Sr Programmer Analyst- CDISC SDTM (remote)
Company: Thermo Fisher Scientific
Location: Morrisville
Posted on: March 19, 2023
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Job Description:
Are you ready for an amazing opportunity that truly will make a
difference, with an amazing team and incredible leadership? If so,
you are in the right place! We are vital links between an idea for
a new medicine and the people who need it. We are the people of PPD
clinical research services - thousands of employees in locations
worldwide connected by tenacity and passion for our purpose: to
improve health
(https://www.ppdi.com/about/purpose-mission-strategy) . You will be
joining a truly collaborative and winning culture
(https://www.ppdi.com/careers/about/culture) as we strive to bend
the time and cost curve of delivering life-saving therapies to
patients. The Data Transformation and Submission (DTS) group within
our Biostatistics & Programming department performs active global
CDISC submission development for clients in our Biotech, Biopharma
and FSP groups. There is also responsibility for Spotfire
exploration, SDTM, DSUR reporting, eCRT (Define.xml) as well as
cross functional development initiatives with various internal
departments, including CDM, Early Dev Services, PVG, etc. The DTS
group also works on many stand-alone studies that are led and
driven fully within the group. As Senior Programmer Analyst within
DTS, you will perform specification, development, quality
validation and regulatory submission compliance for PPD developed
CDISC SDTM and CDISC eCRT (Define.xml) programming deliverables,
using Windows SAS Grid. You will deploy Spotfire dashboards, Safety
notifications and reporting for Medical Monitor review and
regulatory actions. As a DTS team member, you will be a key team
player for internal Biostatistics interactions and client
engagement on CDISC submission topics, or internal contact for
procedural and technical solutions. We are vital links between an
idea for a new medicine and the people who need it. We are the
people of PPD - thousands of employees in locations worldwide
connected by tenacity and passion for our purpose: to improve
health.?You will be joining a truly?collaborative and winning
culture as we strive to bend the time and cost curve of
delivering?life-saving therapies to patients.?? Our Biostatistics &
Programming (B&P) department are passionate about being data
and technically agile and driving enhanced value for our clients
and patients. Determined to improve patient health, we help PPD
provide industry leading CDISC expertise and programming leadership
through global delivery, consistent quality adherence and
scientific insight. Your responsibilities will include (but are not
limited to) the following: + Creation of specifications,
development, validation, and delivery of CDISC SDTM and regulatory
deliverables (eCRT Define.xml, SDTM aCRF) + Analysing and combining
data from a variety of sources and structures including virtual
trials, wearables, eCOA, etc. + Generating visualizations
(Spotfire), Statistical safety reports (TLFs), safety event
notifications and data alerts for study teams. + Provide consult,
analysis, and support across various therapeutic area studies in
their CDISC compliance and consistency in mapping. + Act as
programming lead on Phase II-IV studies of moderate to high
complexity. + As programming lead working directly with project
team leaders and client representatives and where required to
conduct team meetings, develop, and maintain project timelines,
assess, and forecast resources, and monitor study budgets. +
Develop instructional training and education materials for the
wider B&P community. + Provide mentorship to junior team
members. **Education, Experience and Skills required:** + MS/MA
degree in computer science, statistics, biostatistics, mathematics
or related field and 4-5+ years of experience + In-depth
understanding of SAS and, ideally, one other programming language +
In-depth understanding of relational data base structure and
complex data systems + Capable of effectively capturing
biostatistical metrics + Capable of providing quality control
review for statistical programming and identifying solutions and
process improvements + Capable of independently and effectively
organizing and managing multiple assignments with challenging
timelines + Solid project management skills to act as project lead
across the most challenging and complex projects + Demonstrated
leadership, initiative, and motivation + Capable of training and
mentoring others + Fluent in English EEOC: We are an inclusive
equal employment opportunity company. We value all people
regardless of background, experience and abilities. Below is listed
the working environment/requirements for this role: Able to
communicate, receive, and understand information and ideas with
diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary for typical working hours.
Ability to use and learn standard office equipment and technology
with proficiency. Able to perform successfully under pressure while
prioritizing and handling multiple projects or activities. May
require travel. (Recruiter will provide more details). The salary
range estimated for this position is $109,000-130,000. This
position will also be eligible to receive a variable annual bonus
based on company, team, and/or individual performance results in
accordance with company policy. Actual compensation will be
confirmed in writing at the time of offer. We offer a comprehensive
Total Rewards package that our US colleagues and their families can
count on, which generally includes: + A choice of national medical
and dental plans, and a national vision plan + A wellness program,
and valuable health incentive opportunities for company
contributions to a Health Reimbursement Account (HRA) or Health
Savings Account (HSA) + Tax-advantaged savings and spending
accounts and commuter benefits + Employee assistance program + Paid
Time Off, 10 paid holidays annually, 8 hours of volunteer time,
paid parental leave (3 weeks for bonding and 8 weeks for caregiver
leave), accident and life insurance, short- and long-term
disability, and volunteer time off in accordance with company
policy + Retirement and savings programs, such as our competitive
401(k) U.S. retirement savings plan As well as being rewarded a
competitive salary, we have an extensive benefits package based
around the health and well-being of our employees. We have a
flexible working culture (https://www.ppdi.com/careers/life-at-ppd)
, where PPD clinical research services truly value a work-life
balance. We've grown sustainably year on year but continue to offer
a collaborative environment, with teams of colleagues eager to
share expertise and have fun together. We are a global organization
but with a local feel. Our 4i Values: Integrity - Innovation -
Intensity - Involvement If you resonate with our 4i values above,
and ultimately wish to accelerate the delivery of safe and
effective therapeutics for some of the world's most urgent health
needs, submit your application - we'd love to hear from you!
*LI-KF1 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.
Keywords: Thermo Fisher Scientific, Cary , Sr Programmer Analyst- CDISC SDTM (remote), Professions , Morrisville, North Carolina
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