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- Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. - Influence and
• 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在 研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批 和试验用药品的发放，协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。 • 得到研究者授权后，根据法规和GCP的要求，协助研究者顺利完成方案要求的随访和步骤：如 制定计划、清点核对药品和
Clinical Trial Psych Rater - Italian Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing sc
As a Principal Biostatistician, you will provide strategic statistical leadership for Oncology clinical trials, with a particular focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma. You will work closely with cross-functional teams to deliver h
- Participate in the design and implementation of projects related to Real-World Evidence (RWE), healthcare data analytics, and Artificial Intelligence (AI), including data management, document development, and project support activities. - Support end-to-end project execution an
Key Responsibilities 1. Manage and coordinate day-to-day support activities, independently handle and resolve complex support cases submitted by clinical trial sites; 2. Provide technical support for medical devices and associated applications at clinical trial sites; diagnose an
IQVIA is currently recruiting for Market Access Managers who will be accountable for implementing patient access strategies and tactics with supporting materials, particularly focusing on advanced budgetary notifications and healthcare system preparation, plus pull through for re
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeuticall
The Research Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. Research Coordinators assist with screening patients, schedule, a
Designs or modifies data models to solve complex database requirements considering business and application needs. Organizes metadata for use by teams. - Participate in the development and maintenance of global clinical data standards, including operational (eCRF and non-eCRF (e
- Develop and implement research related to Real-World Evidence (RWE) business areas (observational studies, survey studies, systematic reviews & meta-analysis). - Design and conduct observational studies: protocol development, methodology/statistical analysis plan, feasibility a
Job Overview Acts as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirem
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ma
The Principal Biostatistician will serve as the statistical lead for clinical studies, providing scientific oversight, strategic guidance, and hands‑on statistical support across late‑phase clinical trials. This role requires a highly experienced biostatistician capable of workin
Wil jij mee het verschil maken voor patiënten met chronische luchtwegaandoeningen? Ben je commercieel sterk, bouw je graag duurzame relaties op en voel je je thuis in een wetenschappelijke omgeving? Dan hebben wij een mooie uitdaging voor jou. Voor onze klant, een toonaangevende
Project Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providin
Job Overview Accountable for management and service delivery excellence of a range of large sized regional and global projects as assigned, covering single or multiple Lifecycle Safety functions (clinical trial and / or post-market). Provide leadership and accountability for cust
This is a fully on-site position in Scottsdale, Arizona Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on res
Ben jij een ervaren farmaceutisch afgevaardigde die zowel commercieel als inhoudelijk sterk staat? Krijg je energie van het uitbouwen van duurzame klantenrelaties, het analyseren van marktpotentieel en het behalen van ambitieuze doelstellingen? Dan is deze uitdaging iets voor jou
As a Principal Biostatistician, you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross‑functional stakeholders in a fast‑paced, global environment. • Provide Principal‑level Biostatistics suppo