Clinical Programmer jobs in West Orange, 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 Research Coordinator III
- DM Clinical Research
-
Jersey, NJ
FULL_TIME
-
Clinical Research Coordinator III
A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES- Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- Sponsor-provided and IRB-approved Protocol Training
- All relevant Protocol Amendments Training
- Any study-specific Manuals Training, as applicable
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
- Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
- Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
- Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
- Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
- Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
- Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
- Ability to train and mentor site staff, as needed
- Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
- Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
- Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
- Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
- Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
- Being prepared for and available at all required company meetings.
- Submitting required administrative paperwork per company timelines.
- Occasionally attending out-of-town Investigator Meetings
- Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
- Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
- Facilitate effective communication between patients, healthcare providers, and research staff
- Any other matters as assigned by management
KNOWLEDGE & EXPERIENCE
Education:- High School Diploma or equivalent required
- Bachelor's degree preferred
- Foreign Medical Graduates preferred
- Minimum of 5 years experience in Clinical Research
- Supervisory experience preferred
- Wide therapeutic range of clinical trials experience preferred
- Regulatory research experience is a plus
- ACRP or equivalent certification is preferred
- Goals-driven while continuously maintaining quality.
- Must be detailed-oriented, proactive, and able to take initiative.
- Must have strong written and communication skills.
- Must have excellent customer service skills.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
- Just Posted
Application Programmer
- Genesis10
-
Jersey, NJ
FULL_TIME
- Genesis10 is currently seeking an Application Programmer with our client in the financial industry located in Jersey City, NJ. This is a 12 month contract position. Responsibilities: Assist in the dev...
- 25 Days Ago
Programmer Analyst
- BizTek People, Inc. | APA International Placement Consultants
-
Hoboken, NJ
FULL_TIME
- SUMMARY Senior Associates (Programmer Analysts) develop and maintain client/server and Web based application software by using an appropriate mix of technology stacks (Microsoft, Java and Open Source)...
- 26 Days Ago
OnBase Programmer
- SoHo Dragon
-
Jersey, NJ
CONTRACTOR
- SoHo Dragon represents an investment bank with offices in Jersey City, NJ that needs to hire an OnBase Programmer. Work Schedule - Hybrid (Onsite: 1 or 2 days a week) PRINCIPAL DUTIES AND RESPONSIBILI...
- 29 Days Ago
LabVIEW Programmer
- Stevens Institute of Technology
-
Hoboken, NJ
PART_TIME
- Job Description Prepares computer by installing and modifying system software. Education: Bachelors Degree in a technical field. An individual is sought with experience in developing LabVIEW code for ...
- 1 Month Ago
Mainframe Programmer
- Sonsoft Inc
-
Florham Park, NJ
FULL_TIME
- Company DescriptionSonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Softwa...
- 1 Month Ago
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0 Clinical Programmer jobs found in West Orange, NJ area
Senior Clinical Programmer Analyst
- Infotech Spectrum Inc,
-
Nutley, NJ
- Job Title: Senior Clinical Programmer Analyst Location: Nutley, NJ ( Remote, Consultant need to be in USA) Duration: Lon...
- 4/22/2024 12:00:00 AM
Clinical Programmer Analyst - Senior
- Zenith LifeScience, LLC
-
Nutley, NJ
- Clinical Programmer Analyst - Senior Location: Nutley, NJ (Remote) Duration: 12 Months Responsibilities " Senior Rave Pr...
- 4/22/2024 12:00:00 AM
Clinical Programmer Analyst - Senior
- LanceSoft Inc
-
Nutley, NJ
- Qualifications: Remote Role " Minimum 10 years of relevant work experience to include data management and/or database pr...
- 4/22/2024 12:00:00 AM
Clinical Programmer Analyst - Senior
- LanceSoft
-
Nutley, NJ
- Qualifications: Remote Role •Minimum 10 years of relevant work experience to include data management and/or database pro...
- 4/22/2024 12:00:00 AM
Senior Director, Clinical Development
- Axsome Therapeutics, Inc.
-
New York, NY
- JOB SUMMARY Axsome Therapeutics is seeking a Director of Clinical Development. The Director of Clinical Development is r...
- 4/22/2024 12:00:00 AM
Director Clinical Development
- Insmed, Inc.
-
Bridgewater, NJ
- Company Description Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living ...
- 4/21/2024 12:00:00 AM
Director, Clinical Development - Cardiovascular
- Formation Bio
-
New York, NY
- About Formation Bio At Formation Bio, we are building the pharma company of the future , redefining drug development wit...
- 4/21/2024 12:00:00 AM
Senior Clinical Programmer Analyst (100% Remote role)
- Maxis Clinical Sciences
-
Nutley, NJ
- Job Description Job Description SAS Programmer Analyst Can be 100% remote We need someone with SAS programming skills wi...
- 4/19/2024 12:00:00 AM
About West Orange, New Jersey
West Orange is a suburban[22][23] township in central Essex County, New Jersey, United States. As of the 2010 United States Census, the township's population was 46,207, reflecting an increase of 1,264 (+2.8%) from the 44,943 counted in the 2000 Census, which had in turn increased by 5,840 (+14.9%) from the 39,103 counted in the 1990 Census.[24]
According to the United States Census Bureau, the township had a total area of 12.171 square miles (31.522 km2), including 12.046 square miles (31.198 km2) of land and 0.125 square miles (0.324 km2) of water (1.03%). It is located approximately 5 miles...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Programmer jobs
$72,587 to $92,034
West Orange, New Jersey area prices
were up 1.6% from a year ago
were up 1.6% 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