Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
Global Clinical Trial Manager
Location
New York
Posted
8 days ago
Salary
$95K - $175.7K / year
Seniority
Senior
Job Description
Job Requirements
- Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
- At least (3) years of relevant experience as Global CTM
- Clinical research organization (CRO) and ONCOLOGY therapeutic experience preferred
- Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements
- Strong organizational skills
- Strong ability to manage time and work independently
- Ability to embrace new technologies
- Excellent communication, presentation, interpersonal skills, both written and spoken
- Ability to travel as necessary (approximately 25%)
Benefits
- Health benefits to include Medical, Dental and Vision
- Company match 401k
- Eligibility to participate in Employee Stock Purchase Plan
- Eligibility to earn commissions/bonus based on company and individual performance
- Flexible paid time off (PTO) and sick time
Related Guides
Related Categories
Related Job Pages
More Clinical Research Jobs
The Project Manager is responsible for ensuring the successful delivery of assigned clinical trial projects by aligning study specifications with client and internal requirements, managing scope, timelines, and cross-functional activities. Key duties include leading client meetings, troubleshooting issues related to specimens and compliance, monitoring progress, and maintaining clear communication with stakeholders.
Prin. Clinical Specialist - Superficial Venous Interventions (SVI) - New York City, Long Island, Northern New Jersey
MedtronicMedtronic is a global leader in medical technology, dedicated to improving healthcare through innovative therapies and devices. Known for transforming patient c
The specialist will provide detailed technical support for Superficial Venous Interventions (SVI) products and procedures to clinical staff, including physicians, nurses, and technicians. Key duties involve product training for various audiences on systems like Closure System and VenaSeal, providing case support, and resolving customer complaints.
The Clinical Compliance & Quality Specialist is responsible for ensuring regulatory and quality compliance across clinical operations. This role requires consistent use of independent judgment and discretion in evaluating, auditing, and improving clinical systems and processes. T...
Associate Director, Feasibility
Alnylam PharmaceuticalsWe are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
The Associate Director leads the predictable and competitive delivery of feasibility assessments across clinical trials, ensuring timely, high-quality deliverables that inform protocol design, geographic strategy, and enrollment forecasting. This role involves acting as an expert point of contact for study leaders regarding protocol feasibility, site burden, and patient voice during planning phases.
