We are seeking a Clinical Project Manager to support the sourcing, handling, and management of biological samples and associated clinical metadata from academic collaborators, commercial biobanks, and clinical research centers. This role involves coordinating with suppliers (hospitals/research institutes/biotech companies), regulatory bodies, and internal teams to secure the necessary biological materials for research and development.
The CPM will play a key role in translating internal research needs into actionable collaborations, managing projects end-to-end from feasibility through sample delivery and data return to collaborators.
This role sits within the Cohort Acquisition Team within the Data group and reports to the Senior Clinical Project Manager.
Location: Ramat Gan, Israel (hybrid model)
What will you do?
Manage multiple sample acquisition projects, from initiation through delivery.
Oversee handoff and tracking of samples through internal processing pipelines.
Track milestones, risks, and dependencies across internal and external stakeholders.
Work closely with internal stakeholders to provide regular updates on sample availability, quality, and timelines.
Align expectations across teams and ensure smooth communication.
Support identification and evaluation of potential sources (academic centers, biobanks, CROs) and sample cohorts (cohort availability, sample types, clinical annotations, timelines).
Serve as a day-to-day point of contact for collaborators.
Track and resolve operational issues (delays, quality concerns, missing data).
Maintain clear documentation of project scope, status, and outputs.
Maintain and leverage a database of existing collaborations.
Enforcing quality standards, including complying with our internal standards.
Requirements: Required qualifications:
Bachelor degree in relevant Life Sciences domain - Biology, Chemistry, Nursing, Pharmacy, Public Health, or Health Sciences - a must
1-3 years experience in clinical research, clinical operations, or project management - a must
GCP certificate - an advantage
Understanding of applicable regulations and practices in clinical trials (such as consent and IRB) and data privacy, (such as,HIPAA, GDPR) and other standards related to biological sample procurement and conducting of observational clinical studies - an advantage
Excellent organizational and communication skills to handle complex sample procurement processes and vendor relationships
Strong attention to detail and quality
Proactive problem-solving and ownership mindset
Project management certification - an advantage
Fluent English - a must
Desired personal traits:
You want to make an impact on humankind
You prioritize We over I
You enjoy getting things done and striving for excellence
You collaborate effectively with people of diverse backgrounds and cultures
You have a growth mindset.
This position is open to all candidates.