Project Manager
Massive BioTurkey14 days ago
Full-timeProject Management, Information Technology
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Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of location or financial situation. Our proprietary patient recruitment and enrollment enablement solution for oncology clinical trials solves every friction point in traditional clinical trial enrollment. Privately held and headquartered in Boca Raton, FL, our passionate change-making team is looking for a Project Manager.
About The Role
We are seeking a highly motivated Project Manager to join our Operations & Customer Success team at Massive Bio. The ideal candidate will play a pivotal role in managing the clinical trial patient journey, driving cross-functional collaboration, and ensuring high-quality deliverables for our clients and partners. This position offers a unique opportunity to contribute to cutting-edge clinical trials in oncology and hematology while gaining international experience in a rapidly growing biotech environment.
Key Responsibilities
Education
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About The Role
We are seeking a highly motivated Project Manager to join our Operations & Customer Success team at Massive Bio. The ideal candidate will play a pivotal role in managing the clinical trial patient journey, driving cross-functional collaboration, and ensuring high-quality deliverables for our clients and partners. This position offers a unique opportunity to contribute to cutting-edge clinical trials in oncology and hematology while gaining international experience in a rapidly growing biotech environment.
Key Responsibilities
- Manage clinical trial programs end-to-end, including trial funnel management and patient acquisition channels
- Collaborate cross-functionally with Marketing, Provider Engagement, and Clinical Operations teams to optimize patient experience
- Prepare and maintain weekly/monthly reports to track client success metrics and project progress
- Oversee action item management, ensuring timely follow-up and completion of tasks arising from client meetings and sponsor requests
- Draft, update, and maintain regulatory letters, track patient status, and prepare client-facing presentation materials
- Ensure accurate documentation of trial facility details and updates in internal CRM and EMR systems
- Contribute to continuous improvement of operational workflows to enhance efficiency and client satisfaction
Education
- Bachelor’s degree from a top-tier university with strong academic achievement in one of the following majors:
- Medicine, Pharmacology, Molecular Biology & Genetics, Biology, Chemistry, Chemical Engineering
- Graduates in Business Administration/Management, Economics, Industrial Engineering, or Statistics are welcome if supported by a Master’s degree in Life Sciences with physiology and pharmacology knowledge
- Minimum 2 years of experience in an international pharmaceutical, healthcare, or biotechnology company, preferably in a Project Manager or Product Manager capacity
- Prior experience in CROs or clinical trial management is a significant asset
- Demonstrated experience with CRM tools (e.g., HubSpot, Salesforce)
- Strong proficiency in Microsoft Office Suite (Excel, PowerPoint, Word, Outlook)
- Essential understanding of human physiology; knowledge in oncology and/or hematology is a plus
- Fluency in English (C1.3 or above); additional languages are an advantage
- Knowledge of HIPAA and GDPR compliance is a plus
- Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced environment
- No travel restrictions
- Exposure to cutting-edge clinical trials in oncology and hematology
- An opportunity to grow within a fast-paced international biotechnology company
- Collaborative environment with a mission-driven culture focused on patient access to innovative therapies
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Key Skills
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