Clinical Site Payments Analyst

**Career Opportunity**We are seeking a skilled Clinical Site Payments Analyst to join our team at Allergan Aesthetics.This role offers the opportunity to work with a dynamic team, develop analytical and problem-solving skills, and contribute to the success of our global clinical site payments operations.**Key Responsibilities and Requirements:**Managing CSAs...

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and...

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and...

**Job Description**The Clinical Site Payments Analyst is responsible for managing global clinical site payments from contract execution through reconciliation.This role requires strong analytical, operational, and customer-centered skills to support all clinical payment stakeholders and internal team members.**Responsibilities Include:**Managing CSAs to...

**About Us**We're a global leader in clinical research services, helping pharmaceutical companies bring new treatments to market. Our mission is to shape the future of clinical development by delivering innovative solutions that drive patient outcomes.**Job Title:** Senior Contract and Budget Analyst**Job Summary:** We're seeking a seasoned professional to...

WHAT TO EXPECT We are looking for a Functional Analyst with experience in the banking sector and knowledge of the payments domain . The candidate will join a team supporting our banking clients in their transformation initiatives, focusing on international and cross-border payments. Analyze business requirements and ensure they align with client needs...

We're currently looking for a **Clinical Trial Coordinator** able to collaborate at local level closely with COM, CRM and CRA, in addition with finance/budgeting representatives to manage CTRAs and payments.**Responsibilities include, but are not limited to**:- Track (e.g.essential documents) and report (e.g.Safety Reports)- Ensure collation and distribution...

Job Description: The position includes a diverse set of duties. In addition to your critical role in overseeing and managing clinical trials, you will take on advanced proctoring responsibilities As a Clinical Specialist, you will train study site staff on the correct use of the study device and provide input during live cath lab procedures. Periodic...

Job Description: The position includes a diverse set of duties.In addition to your critical role in overseeing and managing clinical trials, you will take on advanced proctoring responsibilities As a Clinical Specialist, you will train study site staff on the correct use of the study device and provide input during live cath lab procedures.Periodic technical...

We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Preference will be given to candidates based in or around Rome, Pisa, Livorno, Grosseto , or Florence . Job Requirements: Bachelor's degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of onsite monitoring...

We are looking for aPart-Time Freelance CRAto strengthen our clinical operations inItaly.Preference will be given to candidates based in or aroundRome, Pisa, Livorno, Grosseto , orFlorence . Job Requirements: Bachelor's degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of onsite monitoring...

We are looking for aPart-Time Freelance CRAto strengthen our clinical operations inItaly.Preference will be given to candidates based in or aroundRome, Pisa, Livorno, Grosseto , orFlorence .Job Requirements: Bachelor's degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of onsite monitoring...

Job DescriptionFor our Campoverde site, we are looking for a Clinical Site Contracting Manager (MCSC), responsible for ensuring that contracts required for Clinical Studies are executed in a compliant and timely manner. This position works both independently and in collaboration with other leaders, to implement the clinical contracting strategy and ensure...

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.We bring a human touch to...

CliniRx has a number of CRA positions available to support a global study in Q1 2025. We are expanding at a rapid rate and have multiple opportunities on a permanent basis to join us on a global study. Ideally, you will come from a CRO background with experience across multiple therapeutic areas. As a global contract research organization (CRO), we offer a...

As a Site Management Lead at Merck Gruppe - MSD Sharp & Dohme, you will play a critical role in ensuring the success of our clinical research studies.About the RoleYou will be responsible for managing site performance and patient recruitment, while ensuring compliance with ICH/GCP and country regulations, as well as company policies and procedures. You will...

The role of Clinical Research Associate is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements...

The Clinical Research Associate is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and...

At Merck Gruppe - MSD Sharp & Dohme, we are seeking a highly skilled Clinical Research Associate to join our team.About the RoleThe successful candidate will be responsible for ensuring compliance with ICH/GCP and country regulations, as well as company policies and procedures. They will act as the primary site contact and site manager throughout all phases...

About the Role:You will lead a high-performing team responsible for managing clinical studies across Italy. Your expertise in clinical trial management and site monitoring will be essential in driving operational excellence and ensuring compliance with regulatory requirements.Main Accountabilities:Develop and implement effective clinical study strategies to...