senior clinical analyst Jobs

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Clinical - Pharmacist 1

Pyramid Consulting, Inc.

Remote

Contract

Immediate need for a talented Clinical - Pharmacist 1. This is a 03+ months contract opportunity with long-term potential and is located in TX(Remote). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-71390 Pay Range: $60 - $65/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: The main function of a pharmacist is to

Clinical Application Support

Beacon Hill

Philadelphia, Pennsylvania, USA

Full-time

Location: Philadelphia, PA (4 days on site, 1 day remote) Salary: 75-80K We are seeking an Application Support Specialist with clinical industry experience to provide comprehensive technical support for clinical devices and applications. This role requires strong knowledge of clinical systems, field support, clinical data management, and configuration management. You will work closely with cross-functional teams to troubleshoot, resolve, and optimize clinical applications and devices to ensure

Regulatory/Clinical Coordinator (HYBRID)

NetSource, Inc.

Denver, Colorado, USA

Contract

Please note that this is a 6 to 12-month contract position. Only local candidates need to apply. Can work remotely as long as the candidate is local to Denver, Frederick, or Boulder, Colorado. Experience with preparing or reviewing sections of an IND or NDA Any mention of work in CMC (Chemistry, Manufacturing, and Controls) key search term Exposure to drug development beyond just clinical responsibilities Familiarity with components of regulatory submissions, especially CMC sections Candidates

Clinical Business Operations Associate

Informatic Technologies

Remote

Contract

One of our leading Pharmaceutical client is looking to hire a Clinical Business Operations Associate in Morristown, NJ. Position Summary: The role of the Clinical Business Operations Associate is to review and approve invoices and expenses against contracts established with the Research and Development function of Clinical Operations globally. Additionally, support and manage a variety of clinical contracts, various contract administrative and legal matters as needed. This role can work from Cli

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe

Clinical Pharmacologist

Sunrise Systems, Inc.

Remote

Contract

Job Title: Clinical Pharmacologist Job ID: 25-07547 Location: 100% REMOTE Duration: 06 months on W2 Contract Description: Director, Clinical Pharmacology Virtual(via Kendall Square, Cambridge, MA) This contractor will serve as a back up to the internal FTE on projects. This individual will support the PK/PD aspects of clinical studies (from protocol to CSR) and related regulatory submission activities. This role requires a strong pharmacokinetics/pharmacodynamics/pharmacometrics knowledge.

Program Manager with healthcare, med-tech, or optometry/clinical workflow knowledge.

Valueprosite

Dallas, Texas, USA

Third Party, Contract

Candidates must be local to Dallas, TX. Candidate profiles should align closely with the Optometry & Key Account Partnerships role. Here's the brief JD they should match: Strong project ownership and strategic planning experience. Proven executive engagement skills, working with C-level stakeholders. Cross-functional leadership across business, IT, operations teams. Strong background in risk management, compliance, and quality assurance. Excellent reporting and executive-ready communication skil

Data Engineer (SQL, Python, AI/ML, Snowflake, biostatistics, clinical trial, Imaging)

Diligente Technologies

Sunnyvale, California, USA

Contract

Summary: We re seeking a Data Engineer with strong SQL and Python skills to build and maintain data pipelines supporting clinical enrolment analytics. You ll work closely with data scientists and analysts to ensure clean, scalable, and reliable data systems. Note: Background in clinical trials, biostatistics, Imaging, or healthcare data is must have. PRINCIPAL RESPONSIBILITIES: Must-Have Skills: Advanced SQL and Python (data manipulation, ETL/ELT).Strong understanding of data engineering best pr

Clinical Data Lead - Vaccines

Sanofi U.S.

Morristown, New Jersey, USA

Full-time

Job Title: Clinical Data Lead - Vaccines Location: Morristown, NJ About the Job The Clinical Data Lead adapts and coordinates the data management strategy during development and conduct of clinical studies/projects for the mRNA/vaccine team within Sanofi. In addition, the Clinical Data Lead ensures data integrity and quality for clinical studies in order to deliver a comprehensive clinical database, and contributes to the optimization of data management processes and innovations. We are an i

Director 2, Clinical Engineering - G

Next Step Systems

Zanesville, Ohio, USA

Full-time

Director 2, Clinical Engineering We are seeking an experienced individual for a Director 2, Clinical Engineering opening in Zanesville, OH. The Director 2, Clinical Engineering will oversee numerous types of medical equipment, offer hands-on experience, and provide leadership and process-improvement knowledge to staff. The Director 2, Clinical Engineering should be a high-level leader that can manage a team of supervisors and technical professionals. This is a fantastic opportunity for any acco

Clinical Lead, I&I

Sanofi EU

Cambridge, Massachusetts, USA

Full-time

Job Title: Clinical Lead, I&I Location: Cambridge, MA or Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. The Clinical Lead is the primary clinical lead for a clinical development program, reporting into the Global Project Head (GPH), and leading a team of Clinical Research Directors and C

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal all stu

QA Clinical Supplies Specialist

Zachary Piper Solutions, LLC

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel

IT Product Manager - Clinical Systems

Eli Lilly and Company

Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Director, Engineering - Clinical and Platform Secondary Packaging

Amgen Inc

Remote or Thousand Oaks, California, USA

Full-time

Career Category Engineering Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients ea

Clinical Data Associate

Eli Lilly and Company

Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Data Owner - Manager, Clinical Supply Chain Data

Johnson & Johnson

Remote or Hopewell Township, New Jersey, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m