Freelance Clinical Research Associate

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...

**Join us in our exciting journey!!**: We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond...

**Join us in our exciting journey!!**: We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond...

The **Initiation Clinical Research Associate (iCRA)** specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA I can also support protocol amendments if applicable. This...

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...

At Premier Research, we help biotech and specialty pharma companies transform life-changing ideas into reality. What we do is profoundly connected to saving and improving lives, and we recognize our staff members are the most valuable asset in delivering success. Inspiring and nurturing staff to do their best work means a better, healthier future for all....

The Project Coordinator works with Project Managers, Clinical Trial Managers, Site Selection Team and Clinical Research Associates (CRA) to provide administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical trial lifecycle. As a Project Coordinator, you will take the lead to...

**Who we are and what we do** Deel is a global team that helps businesses hire anyone, anywhere, easily. Deel consists of more than two thousand self-driven individuals spanning over 100 countries. Our unified yet diverse culture keeps us continually learning and innovating the Deel platform and our products for customers. Companies should be able to hire...

**Associate Study Start-Up Manager** **IQVIA Biotech** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Essential Functions**: - Oversee the execution of Site...

**Overview - **Associate Principal - Patient Centered Solutions, CNS Practice**: To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS CNS research...

**Job Overview** CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the relationship management and communication of medical and scientific...

The Manager, Regulatory Affairs is responsible to ensure the services provided by the regional regulatory affairs department are conducted according to Innovaderm’s standard operating procedures, applicable regulations and good clinical practices and to the Sponsor’s satisfaction. Responsibilities include providing leadership on regulatory activities...

**Join us on our exciting journey!** This is a brilliant opportunity for an **Associate Director of Statistical Programming** or **Senior Statistical Programmer with at least 3 years experience** **in a leadership role** to join an exceptional and dynamic programming group. **UK visa sponsorship is NOT available for this role.** The vision of our...

**Join us in our exciting journey!!**: We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond...

**Job Overview** Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. **Essential Functions** - Complete appropriate therapeutic, protocol and clinical...

As a Clinical Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **We are looking for experienced Project Managers with substantial experience in multi-country/global PM experience.** **What you will be doing**: - The Study Manager has responsibility 1 or more...

Resident Advisor is the world’s foremost platform for discovering electronic music, artists and events. Described by the NY Times as “the most influential electronic music site in the world”, every month RA reaches more than 5m people across its web, mobile and app properties. We are looking for a freelance product manager to support the product team...

Parexel is hiring an Launch Excellence Lead to work remotely from the following countries: - Spain - Belgium - Bulgaria - Hungary - Italy - Netherlands - Serbia - United Kingdom**Title**:Associate Director/Director/Senior Director, Launch Excellence Lead (LEL)**Accountability and Supporting Activities** **Project Delivery Management and Oversight** -...

Spain, Remote **Job ID** R0000014735 **Category** Clinical Trials **ABOUT THIS ROLE**: **Position Purpose**: - The Senior Study Manager (SSM) has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies - The SSM leads and manages the tactical execution of one or more...

**Join us on our exciting journey!**: **Position Purpose**: We are looking for a Italian Native Speaker to join us at our Madrid Production Hub office! Your primary focus will be to be responsible for building up a panel of doctors to participate in our researches, follow up of the questionnaire sent and maintaining updated data of Healthcare Professionals...