Clinical Programmer jobs in Plainfield, NJ
Clinical Programmer evaluates, develops, and maintains clinical database and analyzes clinical data. Codes, tests and documents databases. Being a Clinical Programmer performs data validation and develops algorithms for data management, typically using SAS programming language. May require a bachelor's degree. Additionally, Clinical Programmer typically reports to a supervisor or manager. The Clinical Programmer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Clinical Programmer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Programmer jobs
Clinical SAS Programmer
- Katalyst Healthcares & Life Sciences
-
South Plainfield, NJ
CONTRACTOR
-
Responsibilities:
- Develop, validate, and maintain SAS programs for clinical data analysis, reporting, and submission in adherence to CDISC standards, regulatory guidelines, and company SOPs.
- Lead the programming activities for regulatory submissions, ensuring timely and accurate delivery of high-quality datasets, tables, listings, and figures (TLFs).
- Collaborate closely with biostatisticians to generate analysis datasets, perform statistical analyses, and contribute to the interpretation and presentation of study results for submission.
- Ensure data quality and integrity by conducting thorough quality control (QC) checks and implementing appropriate validation procedures.
- Provide expertise in CDISC standards (SDTM and ADaM) and contribute to the development and implementation of data standards and submission deliverables.
- Bachelor's or master's degree in a relevant field such as computer science, statistics, or life sciences.
- Minimum of 5 years of experience as a SAS programmer in the pharmaceutical or biotechnology industry, with a strong focus on oncology clinical trials and regulatory submissions.
- Extensive expertise in SAS programming, including data manipulation, analysis, and reporting.
- Proven experience working with CDISC standards (SDTM and ADaM) and implementing these standards in clinical trials and regulatory submissions.
- Strong understanding of regulatory guidelines (e.g., FDA, EMA, ICH-GCP) governing the analysis and reporting of clinical trial data for regulatory submissions.
- Proficiency in statistical programming using SAS, including experience with SAS/Base, SAS/STAT, SAS/Macro, and SAS/Graph.
- Excellent problem-solving skills, attention to detail, and the ability to work independently in a fast-paced environment.
- 1 Month Ago
Clinical SAS Programmer (CPT/OPT)
- Katalyst Healthcares & Life Sciences
-
South Plainfield, NJ
FULL_TIME
- Company DescriptionKatalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We have ...
- 1 Month Ago
Clinical Social Worker LCSW
- Clinical Management Consultants
-
Edison, NJ
FULL_TIME
- A fantastic opportunity for a Clinical Social Worker LCSW is now available, joining a reputable New Jersey health system. This highly accredited health system offers an array of specialized hospitals ...
- 17 Days Ago
Clinical Research Coordinator I
- DM Clinical Research
-
Jersey, NJ
FULL_TIME
- Lab TechnicianThe Lab Technician will be responsible for assisting the clinical research staff in conducting clinical research trials.Duties & Responsibilities:Prepares, processes, and ships laborator...
- 4 Days Ago
Onsite Programmer
- Expert In Recruitment Solutions
-
Woodbridge, NJ
CONTRACTOR,FULL_TIME
- Title- Onsite Programmer Location- Onsite in Augusta, Maine Duration- 12 months contract Candidates MUST be currently living in the area (this manager will not allow us to send anyone not currently li...
- 19 Days Ago
Statistical Programmer
- Katalyst Healthcares & Life Sciences
-
Rahway, NJ
FULL_TIME
- Responsibilities: Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies. Provide statistical oversight...
- 4 Days Ago
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0 Clinical Programmer jobs found in Plainfield, NJ area
About Plainfield, New Jersey
Plainfield is a city in Union County, New Jersey, United States, known by its nickname as "The Queen City." As of the 2010 United States Census, the city's population increased to 49,808, its highest ever recorded population in any decennial census, with the population having increased by 1,979 (+4.1%) from the 47,829 counted in the 2000 Census, which had in turn increased by 1,262 (+2.7%) from the 46,567 counted in the 1990 Census.[21]
The area of present-day Plainfield was originally formed as Plainfield Township, a township that was created on April 5, 1847, from portions of Westfield Towns...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Programmer jobs
$72,073 to $91,382
Plainfield, New Jersey area prices
were up 1.5% from a year ago
were up 1.5% from a year ago
What does a Clinical Programmer do?
Clinical Programmer in Santa Ana, CA
A clinical programmer works with a staff during clinical trial testing, quite often in the medical field.
December 12, 2019
Clinical Programmer in Austin, TX
Created SAS datasets of clinical data from clinical databases; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms and other software packages; prepared data to be sent to clients.
December 11, 2019
Clinical Programmer in Greenville, MS
Responsibilities shown on sample resumes for this position include reviewing shell data displays for consistency of CRF, importing raw data to SAS datasets, and converting clinical study datasets to conform with CDISC/SDTM standards.
January 30, 2020