- EBS/BA/MS/Ph.D. in Life Sciences with 2+ yrs relevant clinical research experience
- Pharmaceutical and clinical drug development experience in a Clinical Scientist role
- Proven ability to effectively manage multiple complex studies
- 2 years of Medical Monitoring experience required
- Oncology experience preferred
- Aggregate Data Review experience required
- Excellent Excel and PP skills required
- Excellent written and oral communication skills
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Clinical Scientist, FSP
16 minutes ago
Fortrea Durham, United StatesAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and techn ...
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IQVIA Durham, United StatesWork with one of our preferred clients Our client is a leading pharmaceutical/biotech company dedicated to advancing medical science and improving patient outcomes through the development of innovative therapeutics. Their research-driven organization focuses on discovering, devel ...
Clinical Scientist, FSP - Durham, United States - Fortrea
Description
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Clinical Scientist, FSP - Support
Remote
This is a role that involves leading a trial and overseeing medical monitoring. This is not a laboratory scientist role.
In this role, the selected candidate will assist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management; may support a single study or multiple studies; may lead a study with limited scope (e.g., Survival Follow-up); and may interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives.
Education/Qualifications
Experience:
Pay Range: $100,000 - $150,000 USD
Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.
We are accepting applications on an ongoing basis, there is no deadline.
#LI-Remote
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
