Employer Industry: Biopharmaceutical

Why consider this job opportunity:
- Salary up to $145,000
- Opportunity for rapid career advancement for strong performers
- Flexible paid time off (PTO)
- Robust and market-competitive compensation and benefits package, including performance bonuses and equity
- Collaborative and fast-paced work environment that inspires high performance
- Commitment to Diversity, Equity & Inclusion

What to Expect (Job Responsibilities):
- Collaborate with the Senior Clinical Trial Manager to support all aspects of clinical studies, including initiation, planning, execution, maintenance, and close-out
- Act as a liaison between the employer and clinical study sites, fostering strong relationships
- Provide oversight of contract vendors and Clinical Research Organization activities to ensure compliance with study plans and regulations
- Proactively identify and escalate issues, participating in problem-solving and risk mitigation
- Coordinate and maintain tracking systems for subject screening, enrollment, and related metrics

What is Required (Qualifications):
- Bachelor’s degree in natural or health sciences or relevant industry experience
- Minimum 4-6 years of experience within clinical operations or as a study coordinator
- Knowledge of clinical trial documentation and regulatory requirements related to trial master files
- Effective communication and interpersonal skills, with the ability to collaborate in a remote environment
- Strong decision-making abilities and attention to detail

How to Stand Out (Preferred Qualifications):
- Citi training preferred
- Experience working with CROs and vendors
- Familiarity with clinical trial documentation and regulatory requirements
- Eagerness to learn and manage multiple tasks simultaneously
- Proficiency in MS Office Suite (Excel, Word, PowerPoint)

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We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.