38 safety scientist global patient safety iv jobs found

job summary: As a Real-World Data (RWD) Scientist , you will be part of a team powering data driven insights that lead to better, faster decisions and therapies for our patients. Acting as a lead data scientist in your project area, you will contribute RWD expertise to broader cross-functional initiatives. Candidates should be excited to drive innovation by implementing new business technology solutions that solve significant scientific or business proble

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that

job summary: Title: Global Case Management Specialist Location: Remote Reports to: Sr. Manager, PV Operations Global Case Management The Global Case Management Specialist will be responsible for effective execution of the activities of triage, processing, and quality control of individual case safety reports (ICSR) from clinical trials to ensure timely and accurate assessment of adverse event reports. This role will focus on accurate case entry and w

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco

job summary: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled

job summary: Randstad Digital is seeking a Full Stack Developer to support development of an internal application, which is part of a long-term project. Required Skills - MicroServices Development.NET Core (C#)React DevelopmentTypeScriptKafka, Pub/Sub, Event based development location: Tampa, Florida job type: Contract salary: $89 - 90 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Responsible for de

job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents

job summary: The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing, designing, and implementing high-priority analytical strategies, clinical oversight, and initiatives. The team is a high-profile high-impact team that works with PPS functions on a range of product initiatives. As a member of the team, you are at the forefront of working with leaders to identify critical priorities and drive high-value

job summary: Our client is looking to add a Project Manager to their team for a project located on the LA General hospital campus in Los Angeles, CA. This is a 12 month contract opportunity that could lead to being brought on for additional projects. This work could potentially be done remotely. The Construction Project Manager manager will be responsible for maintaining the procurement log for construction projects. This role is critical to ensure time

job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight

job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s

job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

job summary: A research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract salary: $38 - 40 per hour work hour

job summary: Seeking a skilled Epidemiologist to execute data analyses, contribute to regulatory deliverables, and design epidemiological studies. Proficiency in SAS / R, real-world datasets, and excellent communication skills are essential. We're looking for a motivated professional with an MPH degree and 2+ years of experience, ready to grow in a dynamic pharmaceutical environment. Flexible, Part time hours (20 hours/week) Fully Remote, any time zone in

job summary: The Staff Quality Engineer, Software will be the subject matter expert on providing guidance to the organization and the software teams in establishing policies and procedures for Software Design Control. This individual will be an integral part of the software development life cycle process in informing, guiding, and evaluating the teams' adherence to practices that would ensure compliance to required regulatory requirements. SKILLS REQUIRED

job summary: 100% remote. MN based is ideal. Hours: Typical hours are 8am CT to 5pm CT, M-F Duration: 5 months. Short term coverage for maternity leave location: Minneapolis, Minnesota job type: Contract salary: $76 - 86 per hour work hours: 8am to 5pm education: No Degree Required responsibilities: Responsibilities: Team Management: Manage a team of product managers/product owners that are supporting delivery of features and

job summary: Randstad Engineering Solutions is looking for qualified system engineers to join our embedded engineering team to support verification efforts of an Integrated Modular Avionics (IMA) platform. . We are looking for system engineers with robust knowledge in DO-178B level A, ARP 4754, ARINC 664 and ARINC 429 with the ability to support coverage analysis efforts across various levels with the project for hardware, software and systems. IMA experi

job summary: One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract sa

job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning

job summary: 100% Telecommute Work Hours: 9am-5pm CST location: Minneapolis, Minnesota job type: Contract salary: $55.00 - 65.50 per hour work hours: 8am to 5pm education: No Degree Required responsibilities: Responsibilities: Develop and manage effective working relationships with other departments, groups, and personnel with whom work must be coordinated or interfacedEfficiently communicate with ETL architect while understan

job summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertise

job summary: Compelling Story & Candidate Value Proposition This position provides candidates the opportunity to work from complex SQL to build UI. Candidate will be solving complex problems due to high volume of data processing. location: Saint Louis, Missouri job type: Contract salary: $53 - 63 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Candidate Requirements Required: Bachelor's degree Preferr

job summary: The ServiceNow CMDB Administrator will provide both daily operational support for the CMDB and coordinate with the Configuration Management Process Lead with the onboarding of new Configuration Item (CI) Classes and CI Class owners into the CMDB process. Daily operational support includes ensuring data accuracy, integrity, and reliability. This involves tasks like managing configuration items, their relationships, and attributes, as well as e

job summary: Hadoop Administrator (24-Month Contract) - ERP Implementation We're seeking an experienced Hadoop Administrator to join our dynamic team on a 24-month contract. In this role, you'll play a crucial part in our enterprise resource planning (ERP) initiatives by managing our Cloudera environment and ensuring optimal performance of our data infrastructure. The Ideal Candidate We're looking for a self-sufficient professional who takes initiative an

job summary: Our West Michigan Client has a contract opportunity for a Technical Product Owner who will take ownership of applications as well as be responsible for working with software developers/ engineers and architects to provide consultative guidance and direction to the team. This role can be remote, located in or near Michigan. location: Grand Rapids, Michigan job type: Contract salary: $48 - 58 per hour work hours: 8am to 5pm educat

job summary: We are seeking a Sr. Data Analyst to join the Clinical Systems Analytical & Reporting (CSAR)-Analytics team within Global Development Operations. This role will enhance our analytical reporting capabilities and support business continuity across multiple clinical system technology enhancement projects. Key responsibilities include contributing to analytics initiatives supporting critical business functions relying on data from eTMF, EDC, CTMS

job summary: The Clinical Evaluations Specialist manages regulatory documentation for MDR remediation and PPRRs, requiring expertise in clinical literature reviews, regulatory writing, and post-market surveillance. This role supports medical device life cycle management and collaborates with cross-functional teams. Foreign-trained ophthalmologists are encouraged to apply. This is a 6-month on-site contract in Duluth, GA, with the potential for extension.

job summary: Our client is a well-known multinational food and snacks manufacturer and they are looking for a high level ERP Transformation Program Manager to join their team on a 12 month contract. The ERP Transformation Program Manager will be brought on to drive a multi-year enterprise resource planning (ERP) transformation initiative across our client's organization. This role will oversee the consolidation of multiple ERP systems into a unified, mode