Fortrea is a premier global Contract Research Organization (CRO) dedicated to scientific excellence with decades of experience in clinical development. We offer comprehensive clinical development, patient access, and technology solutions across more than 20 therapeutic areas to pharmaceutical, biotechnology, and medical device clients. With a team of over 19,000 professionals operating in more than 90 countries, Fortrea is at the forefront of transforming drug and device development for partners and patients worldwide.
Job Description:
The following outlines the general responsibilities and expectations for the role, though it is not an exhaustive list of all duties, skills, and responsibilities:
Adverse Event Management:
Report Submission and Maintenance:
Compliance and Documentation:
Training and Relationship Building:
Additional Duties:
Experience and Qualifications:
Location: Bangalore
Why Join Fortrea?
Fortrea seeks innovative, solution-oriented individuals who are passionate about overcoming challenges in clinical trials. We are committed to revolutionizing the development process to ensure rapid delivery of life-changing therapies. Join our dynamic team to experience a collaborative work environment where personal growth is encouraged, enabling you to make a global impact. For more information, visit www.fortrea.com.
Equal Opportunity Employer:
Fortrea is an Equal Opportunity Employer committed to diversity and inclusion. We do not tolerate harassment or discrimination of any kind. Employment decisions are based on business needs and individual qualifications, without regard to race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family status, sexual orientation, gender identity, age, veteran status, disability, or any other legally protected characteristic. We encourage all qualified candidates to apply.
For details on how we handle your personal data, please review our Privacy Statement.
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