Clinical trial management system Jobs

21 - 40 of 210 Jobs

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement

Hospital Clinical Program Manager - clinical in hospital inpatient setting.Job Title - Hospital Clinical Program Manager - clinical in hospital inpatient setting.

APN Software Services, IncCompany Name - APN Software Services, Inc

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Newport Beach, California, USA

Full-time

Please contact Abdul on "" OR email me at "" 2 Openings for Quality Management Team - Roles are very specific - candidates must have in-depth experience in Clinical Quality Improvement in a hospital inpatient setting. Contract to Hire / Direct Hire opportunities for the right talent. 100% Onsite *Candidates must possess all 4 of the below or they will not be considered: 1. Completed PI training and certification (six sigma, lean, CPHQ, Masters in Improvement) from nationally recognized organiza

Clinical Application SupportJob Title - Clinical Application Support

Beacon HillCompany Name - Beacon Hill

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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

Clinical - Pharmacist 1Job Title - Clinical - Pharmacist 1

Pyramid Consulting, Inc.Company Name - Pyramid Consulting, Inc.

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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 SupportJob Title - Clinical Application Support

Beacon HillCompany Name - Beacon Hill

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Philadelphia, Pennsylvania, USA

Full-time

Clinical Business Operations AssociateJob Title - Clinical Business Operations Associate

Informatic TechnologiesCompany Name - Informatic Technologies

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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 ProgrammerJob Title - SAS Clinical Trails Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

Regulatory/Clinical Coordinator (HYBRID)Job Title - Regulatory/Clinical Coordinator (HYBRID)

NetSource, Inc.Company Name - NetSource, Inc.

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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 Research AssociateJob Title - Clinical Research Associate

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Remote

Full-time

Piper Companies is seeking a Clinical Research Associate (CRA) with experience in Oncology clinical trials to join a reputable clinical research organization. This is a full-time/permanent opportunity. Some travel is required (regionally, about 8-10 days out of the month). Candidates must be located in CST or PST in one of the following states: WY, CO, KS, WI, IN, OH, MN, MO, IL, MI, KY, AR, CA, OR, WA, NV, UT, AZ. Responsibilities of the Senior Clinical Research Associate (CRA): Perform site s

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

ValueprositeCompany Name - Valueprosite

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Dallas, Texas, USA

Contract, Third Party

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

Clinical Data Lead - VaccinesJob Title - Clinical Data Lead - Vaccines

Sanofi U.S.Company Name - Sanofi U.S.

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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

Senior Clinical Research Scientist - Diabetes Care (on-site)Job Title - Senior Clinical Research Scientist - Diabetes Care (on-site)

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Alameda, California, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Yo

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

DOC - Clinical Informatics Analyst - 6900 Atmore Drive Richmond, VA - 4 days/week ON SITE. Parking not provided.Job Title - DOC - Clinical Informatics Analyst - 6900 Atmore Drive Richmond, VA - 4 days/week ON SITE. Parking not provided.

Lorven Technologies, Inc.Company Name - Lorven Technologies, Inc.

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Richmond, Virginia, USA

Third Party, Contract

Role: DOC - Clinical Informatics Analyst - One ROLE. IN PERSON IVS ONLY! Job ID - (759856) Location: 6900 Atmore Drive Richmond, VA - 4 days/week ON SITE. Parking not provided. DO NOT SUBMIT CANDIDATES THAT WERE PREVIOUSLY SUBMITTED TO 755397. Job Type : Contract Interview process: In Person Only Job description: **The proper candidate will have experience in a recognized Electronic Health Record system. Our vendor is a Corrections specific vendor, thus we do not expect candidates to be famil

Clinical PharmacologistJob Title - Clinical Pharmacologist

Sunrise Systems, Inc.Company Name - Sunrise Systems, Inc.

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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.

Clinical Lead, I&IJob Title - Clinical Lead, I&I

Sanofi EUCompany Name - Sanofi EU

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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

Director 2, Clinical Engineering - GJob Title - Director 2, Clinical Engineering - G

Next Step SystemsCompany Name - Next Step Systems

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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 Project ManagerJob Title - Clinical Project Manager

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Alameda, California, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Clinical Project Manager Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your tru

Clinical Data ManagerJob Title - Clinical Data Manager

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Alameda, California, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Clinical Data Manager Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true s

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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