Senior Clinical Research Associate - Oncology - Romania - FSP at Parexel

, , Romania -

Full Time

Start Date

Immediate

Expiry Date

23 Jan, 26

Salary

0.0

Posted On

25 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Oncology, Site Monitoring, ICH GCP Compliance, Time Management, Social Skills, Attention to Detail, Regulatory Submissions

Industry

Pharmaceutical Manufacturing

Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do. Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people. Parexel FSP is looking for a Senior Clinical Research Associate in Romania to strengthen our clinical operations team. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience. As a SM, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact. You will possess: Bachelor's degree in a life science or related discipline. Minimum of 3 years' experience in independent site monitoring and in oncology. Understanding of ICH GCP Compliance. Excellent time management and social skills Highly motivated with a phenomenal eye for detail. Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling ~2-3 days/week Current driver’s license required Send me your updated resume to marta.kuniewicz@parexel.com for an immediate interview. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.

Responsibilities

As a Senior Clinical Research Associate, you will be responsible for setting up and overseeing studies, completing study status reports, and maintaining study documentation. You will also participate in the submission of protocols and assist in regulatory submissions.