Clinical Research Associate

Requisition Number: 7739 Position Title: Senior Clinical Research Associate External Description: Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications –...

Tengo varios puestos como Clinical Research Associate en Madrid en los que no es necesaria experiência en industria o CROs, por tanto, si eres un CRA con al menos 1.5 años de experiência que quiere dar el salto y empezar a trabajar en CROs, con lo que ello conlleva (mejora de condiciones, flexibilidad de poder trabajar desde casa o office based, apoyo...

**Job Description**: We are a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where our company has codified its 125-year legacy. Our company' success is backed by...

To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of...

At AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. The Associate Director Clinical Research (ADCR) is responsible for delivering the committed part of all clinical...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality...

Tengo un par de vacantes como Senior CRA en CRO donde aceptan CRA que no tienen experiência en CRO, este es el rol perfecto para aquellos que estéis trabajando en fundaciones u hospitales y queráis dar el paso e ir a CRO. La empresa ofrece un salario muy competitivo junto con beneficios e incluso una bonificación anual. Buscan a gente para trabajar...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Job summary**: As a **Clinical Project Administrator, **you will be expected to provide clerical support to project team and assist in project management activities working with Project Managers. You will be involved in key activities, such as collecting and submitting documents to Regulatory Authorities and Ethics Committees. Additionally, you will be...

**Senior Site Manager, Early Development & Clinical Pharmacology**: We are looking for a Senior Site Manager, Early Development & Clinical Pharmacology (ED&CP) to serve as the primary contact point between the Sponsor and the Investigational Site for the conduct of complex early development and/or clinical pharmacology studies. In other organisations, the...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Assistant. This role, **with an immediate start for 3...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,600 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Majadahonda - Onsite Clinical Research Assistant - part time contract (12h per week) with IQVIA** Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and...

**Job Title**: Associate Director, Clinical Site Contracts **Job Location**: Europe - Remote **Job Overview**: The Associate Director, Clinical Contracts will manage the Clinical Contracts (Legal) team to provide the leadership, support, and guidance to successfully lead a global, company-wide Clinical Contracts team. This position requires an effective...

**Join us in our exciting journey!!** We currently require a motivated, creative and enthusiastic clinical trials professional to join our Site management (SM) division. This role is working in our **sponsor dedicated model**. With a fantastic work/life balance, this is a great opportunity for a Clinical Trials Associate willing to discover what means to...

Job Description SummaryProvides advanced support in clinical research partners in nuclear medicine, with the aim of providing support for early development of new technical and clinical projects, internal validation, project execution support, publication, and integrate regional (mainly Portugal, Spain, Italy, Israel, and Middle East), academic users into...

Job Description Summary Provides advanced support in clinical research partners in nuclear medicine, with the aim of providing support for early development of new technical and clinical projects, internal validation, project execution support, publication, and integrate regional (mainly Portugal, Spain, Italy, Israel, and Middle East), academic users...