
Silverlink Technologies LLC
Roselle, New Jersey • 2d ago
Easy Apply
Contract
50 - 51
12 results (2 new)

Silverlink Technologies LLC
Roselle, New Jersey • 2d ago
Easy Apply
Contract
50 - 51

Amaze Systems Inc
Roselle, New Jersey • Today
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Third Party, Contract
Depends on Experience

Genmab
Princeton, New Jersey • 2d ago
Full-time
USD 131,040.00 - 196,560.00 per year

BridgeBio Pharma
Remote • Today
Full-time
USD 173,800.00 - 217,000.00 per year

Shrive Technologies LLC
Remote • Yesterday
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Contract, Third Party
Depends on Experience

ASCII Group LLC
New York, New York • Today
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Full-time
Depends on Experience
TalentiFi-X LLC
Remote • 14d ago
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Full-time
Depends on Experience

V.L.S. Systems, Inc
Remote • 15d ago
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Contract
Depends on Experience

V.L.S. Systems, Inc
Remote • 14d ago
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Contract
Depends on Experience

ASCII Group LLC
Remote • Yesterday
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Contract
Depends on Experience

Sovereign Technologies
Remote • 9d ago
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Contract
Depends on Experience

We are looking for a Clinical SAS Developer to join our team. Please review the job description below, and let us know if you are interested and available.
If this opportunity matches your experience and career goals, we would love to discuss it more. Additionally, feel free to share your updated resume for consideration
Role: Clinical SAS Developer
Location: Upper Gwynedd, PA /Rahway, NJ
Duration: 12+ Months
Rate: $50/HR on W2
Job Details:
1.Must have 6-8 yrs of exp in clinical domain
2.Strong knowledge of SDTM
3.Create advanced SAS macros, templates, and utilities for efficient data processing
4.Act as the primary programming point of contact for biostatisticians and study teams
5.Perform peer review of code and documentation for accuracy and traceability
6.Review CRF (Case Report Form) annotations and data specifications.
7.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines
Skill:
1.Extensive programming experience in a clinical trial environment (CRO/Pharma).
2.Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
3.In-depth knowledge of CDISC standards and regulatory submission requirements
Thank you!
Best Regards,
Sumit Talekar
Associate Manager – Talent Acquisition
Silverlink Technologies Inc.
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Roselle, New Jersey
•
Today
Clinical SAS Developer - Upper Gwynedd, PA /Rahway, NJ - Onsite Contract position Job description: W2 only. 1.Must have 6-8 yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer review of code and documentation for accuracy and traceability 6.Review CRF (Case Report Form) annotations and data
Easy Apply
Third Party, Contract
Depends on Experience
Pennsylvania
•
Today
HMG America LLC is the best Business Solutions focused Information Technology Company with IT consulting and services, software and web development, staff augmentation and other professional services. One of our direct clients is looking for SAS Clinical Consultant in Upper Gwynedd, PA. Below is the detailed job description. Title: SAS Clinical Consultant Location: Upper Gwynedd, PA Duration: 6 + Months Primary Skills: SDTM, Clinical SAS Job Description: Looking for SDTM experts having in
Easy Apply
Contract, Third Party
$DOE
Princeton, New Jersey
•
2d ago
At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate,
Full-time
USD 131,040.00 - 196,560.00 per year
Hybrid in Pennsylvania
•
Today
Senior Clinical SAS Developer Upper Gwynedd, PA (Onsite) Long Term Contract Employment Type W2 Looking for SDTM experts having in-depth knowledge of SAS programming(macro's) Must have 10+ yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point of contact for biostatisticians and study teams Perform peer review of code and documentation for accuracy and traceability Review CRF (C
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Contract