Manager, Global Tax (United States) - INC Research - Raleigh, NC

Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

At INC Research, we appreciate the complexities of the nervous system and the widely varying disciplines that explore CNS function, dysfunction and drug research. Working with CNS specialists and drawing upon an extensive network of academic and private physician investigators, we have directed clinical trials for more than 20 years in psychiatry, neurology and pain (including indications such as sleep, movement disorders and schizophrenia), earning worldwide recognition as leaders in CNS drug and product development.

We are also experienced at covering vast areas of medical research as such we have become leaders in infectious disease and immunology research, women’s health, and Respiratory diseases Applying our Trusted Process methodology on trials for companies with extensive needs. A career in our General Medicine unit will enable you to work across a variety of therapeutic areas on a diverse range of studies.

We are currently looking to strengthen our Clinical Monitoring team in Spain and are seeking a Clinical Research Associate for our CNS and General Medicine Business Units to be based in our Madrid OR Barcelona office. We can also consider home based workers.

Please note you will be required to have valid right to work in the EU before we can consider your application.

A brief summary of duties you will be involved in:

• Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures


• Data Handling, Reporting, Tracking and administrative tasks


• Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

Qualifications

To succeed in this role you will need the following skills/experience:

• Education – BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position


• Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO


• Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines


• Good command of written and spoken English language

Why choose us: It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry. We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.

“INC Research has been ranked as “Top CRO to work with” among large global CROs in the biannual CenterWatch Global Investigative Site Relationship Survey. INC is the only CRO to rank consistently among the top three CROs in all seven CenterWatch site relationship surveys conducted since 2007”

What happens next: If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.

Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

Primary Location

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Latin America – Mexico, Mexico City – North

Other Locations

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Latin America – Argentina, Buenos Aires, Latin America – Colombia, Bogota, Latin America – Brazil, Rio de Janeiro, Latin America – Peru, Lima, Latin America – Brazil, Sao Paulo, Latin America – Chile, Santiago

Job

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Clinical Operations

Schedule

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Full-time

Travel

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Yes, 50 % of the Time

Employee Status

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Regular