SAS Clinicals Jobs

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Clinical Scientist (Part-Time)

Apex Systems

Cambridge, Massachusetts, USA

Full-time

Job#: 2026161 Job Description: Clinical Scientist (Part-Time) 2026161 Location: Cambridge MA (Hybrid) Science: CRISPR/Cas9 Therapeutic Area: Rare Disease Job Overview: In this role you will collaborate with Clinical Development Physicians and various teams to provide scientific expertise and support in developing and executing clinical development plans, trial designs, protocols, and study-related communications. Primary Job Responsibilities:Design and execute clinical trial activities from pl

Principal Statistical Programmer - Late Phase

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is looking for an experienced Principal/Senior Statistical Programmer to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics. Responsibilities of the Principal/Senior Statistical Programmer: Support Phase II & teams with tasks related to submissions work End-to-End ADaM/TFL efficacy programming Creating submissions packages, eCDT packages, P21 reports, define.xml, SDRG/ADRG, etc. Qualificat

Clinical Database Developer

General Dynamics Information Technology

Frederick, Maryland, USA

Full-time

GDIT's Military Health team is hiring Clinical Database Developer to support the Office of Regulated Activities (ORA) under the DoD (Dept. of Army) located at Ft. Detrick in Frederick, Maryland. The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service,

SAS Programmer (NO C2C)

Juno Search Partners

Philadelphia, Pennsylvania, USA

Contract

Juno Search Partners is a certified women-founded and women-led talent solutions firm with extensive experience in the placement of accounting, administrative, finance, human resources, legal, marketing, operations, and technology candidates nationwide. We are looking for a passionate and experienced SAS Programmer! SAS Programmers are responsible for transforming raw data into analyzing datasets, providing Tables, Listings, and Figures (TLFs), and maintaining and improving analysis algorithms a

Senior Statistical Programmer - PKPD Early Phase

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is looking for an experienced Senior Statistical Programmer (PK/PD) to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics. Responsibilities of the Senior Statistical Programmer: Provide statistical programming expertise in PKPD such as generating ADPC, ADPP and POPPK datasets & NCA TFLs Pooling of PK Parameters and relevant safety ADaM datasets Assist in establishing standardized programming

Medical Director, Drug Safety & Pharmacovigilance

Apex Systems

Cambridge, Massachusetts, USA

Full-time

Job#: 2020686 Job Description: Medical Director, Drug Safety & Pharmacovigilance 2020686 Location: Cambridge MA (Onsite) Science/ Focus: CRISPR/Cas9 Therapeutic Area: Rare Disease Job Overview: This position is well-suited for a Medical Director with substantial expertise in drug development and safety, providing a unique opportunity to strategize the implementation of safety surveillance for clinical trials, oversee the management of safety signals, take charge of cross-functional teams, and co

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Senior Manager, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Senior Manager Biostatistics is responsible for statistical activities in support of clinical trials, including but not limited to the following: contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. You will be responsible for: Collaborates with Clinical Development, Clinical Pharmacology, Regulatory and Clinical Operations expertise are

Senior Clinical Data Manager

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Health and Sciences is actively searching for a Senior Clinical Data Manager to spearhead data management activities with a mid-size Clinical Research Organization (CRO). This is a work from home / remote role. Responsibilities of the Senior Clinical Data Manager: Oversee and perform data management tasks in relation to global clinical trials Manage data management direct reports including clinical data reviewer and coding specialists Work with other team leads and project teams includi

Product Manager Healthcare Insurance

Vega Consulting Solutions

Remote

Full-time

Seeking Candidates with Healthcare Insurance - Product background and experience. Vega Consulting Solutions, Inc. is searching for a Clinical Product Manager for a Remote based, direct permanent job opportunity with our direct client. Prefer candidates that are located on the East Coast. Candidates must be eligible for direct employment. Sponsorship is not available. Reporting to Product and Portfolio Delivery Organization, The Clinical Product Manager will support the clinical and technology te

Principal SAS Programmer

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Companies is seeking a Principal SAS Programmer to work in a fully remote capacity in the US or Canada, and provide statistical programing expertise. This person should be well versed in Phase 1 studies, experienced in generating ADPC, NONMEM datasets, and possess PK/PD experience. You will get to work in a team of high-performing developers to create solutions for a top Clinical Research Organization and their clients. This role is only open for direct-hire, no C2C applicants will be cons

SAS Programmer

Intone Networks Inc.

US

Contract

SAS Programmer Remote Long Term Required: SAS Programmers create, modify, and test the code and scripts that allow computer applications to run. Work from specifications drawn up by software and web developers or other individuals. May develop and write computer programs to store, locate, and retrieve specific documents, data, and information.

Business Analyst - MUST RESIDE IN TEXAS

Luna Data Solutions, Inc.

Austin, Texas, USA

Contract

We are currently hiring an experienced Business Analyst with a deep knowledge of Agile methodologies and SAS Viya. This will be long-term contract in Austin, TX with a hybrid-setting of 3 days onsite and 2 remote. **To be considered, you must currently reside in the Austin Texas metropolitan area.** Requirements: 8 years of in-depth experience / knowledge developing data analysis programs in SAS Viya.5 years of experience in business process visualizations, process improvement, and business syst

SAS Business Intelligence Analyst

Vector Consulting, Inc

Austin, Texas, USA

Contract, Third Party

Our government client is seeking an experienced SAS Business Intelligence Analyst on a hybrid 6+ months renewable contract opportunity inAustin, TX. Role: SAS Business Intelligence Analyst Job Description / Minimum Requirements: Ability to work in hybrid environment and deep knowledge of Agile methodologies and SAS Viya. II.CANDIDATE SKILLS AND EXPERIENCE Minimum Requirements: Candidates that do not meet or exceed theminimumstated requirements (skills/experience) will be displayed to customers

SAS Viya Developer

Allied Consultants, Inc.

Austin, Texas, USA

Contract, Third Party

OverviewAllied Consultants, Inc. is an Austin-based firm which has for 32 years been a premier provider of technical and business professionals to clients in Texas. We are currently seeking an experienced SAS Viya Developerto be a key resource on a technical services team. Allied Consultants offers its family of consultants excellent rates, a local support staff, and an attractive benefits package which includes medical insurance (Allied shares a percentage of the cost), life insurance, a matchi

Sr. SAS Architect must have SAS Architect certification-Onsite - Charlotte, NC

Keylent

Charlotte, North Carolina, USA

Third Party, Contract

*THIS ROLE IS HYBRID in Winston-Salem or Charlotte, NC. 3 days per week in office Job Title: Sr. SAS Architect [SRARCH] Experience: 12 to 15 years Job Summary: Seeking a highly experienced Sr. Architect with 12-15 years of experience in SAS Enterprise Guide and SAS Viya. Roles & Responsibilities: - Should have working experience in SAS suite of products (e.g., Base SAS, SAS/Macros, SAL/ETL, SAS Grid, SAS visual analytics). - Should have worked on SAS 9.4 and SAS Viya - Strong experience workin

SAS Viya Analyst

Voluble Systems LLC

Austin, Texas, USA

Contract

Minimum Requirements: Candidates that do not meet or exceed the minimum stated requirements (skills/experience) will be displayed to customers but may not be chosen for this opportunity. Years Required/Preferred Experience 8 Required Deep knowledge and experience developing data analysis programs in SAS Viya 5 Required At least 5 years of business process visualizations, process improvement, and business system analysis. Thanks & Regards Rajkumar Sharma