Senior Clinical Research Associate

INC Research

Posted: October 27, 2015

Job ID: 137

Job Summary

Term: Full-Time
Job Roles: Clinical Trial Monitoring
Therapeutic Experience: Gastroenterology, Hepatology, Nutrition, Immunology, Infectious Disease, Neurology, Oncology, Respiratory
Required Education: BS/BA or equivalent with solid clinical trial monitoring experience
Required Experience: 2 years

Job Description

Do you want to be 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.

We are currently looking to strengthen our Clinical Monitoring team in North America and are seeking CRA’s of all levels for the following Business Units to be regionally and home-based:

- General Medicine (Infectious Disease, Immunology, GI, Vaccines and Respiratory)
- Oncology (Hematology and Phase I)
- CNS (Alzheimers, Sleep Disorders, Pain, MDD)

Key Responsibilities:
A brief summary of duties you will be involved in:
- Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
- Data Handling, Reporting and Tracking & Administrative tasks
- Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines

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 own our projects, we can take them to new heights.

“We were ranked “Top CRO” to work with in the CenterWatch 2015 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”

We are seeking candidates with the following key attributes:
- Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
- Practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
- Thorough understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
Good command of written and spoken English language

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