Clinical Project Manager

Clinical Project Manager (CPM) – Immediate Opening

Headline: We’re Hiring! Join ABLE-Tx as a Clinical Project Manager (CPM) 🚀

ABLE-Tx, a bio-pharmaceutical startup located in Ramat HaHayal, Tel Aviv, is committed to developing innovative ophthalmic treatments. With our Phase 2 clinical programs advancing, we are seeking a highly experienced Clinical Project Manager (CPM) for an immediate position to drive our trial execution and contribute to our global expansion efforts.

The Role & Evolution: We are currently managing our clinical programs internally without an external CRO. This role offers a unique "hands-on" opportunity to build our clinical foundations. You will lead the direct execution and site management today, and play a pivotal role in the future selection and oversight of external CROs as we scale.

Key Responsibilities:

• Full-Cycle Study Leadership: Lead the execution of clinical trials across Phases I-III, from site feasibility and selection through to study close-out.
• Patient Recruitment Strategy: Develop and implement aggressive recruitment and retention plans—leveraging your deep understanding of site-level bottlenecks to keep studies on track.
• Hands-on Clinical Oversight: Conduct and oversee monitoring activities, ensuring data integrity, protocol adherence, and strict GCP compliance.
• Regulatory & TMF Management: Lead the preparation and maintenance of the Trial Master File (TMF) and manage submissions to Regulatory Authorities and Ethics Committees (IRB/EC).
• Site Relationship Management: Foster high-level partnerships with Principal Investigators and hospital staff to optimize study performance.
• Develop and implement a comprehensive monitoring plan for clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and GCP standards
• Provide targeted training and ongoing guidance to site staff to sustain high standards of conduct, data quality, and patient safety

The Ideal Candidate Profile:

• Must-Have Experience: Proven background as a Clinical Study Coordinator within a medical center/hospital, with a clear understanding of the “inner workings” of a clinical site
• Professional Track Record: Extensive experience as a CPM or Senior CRA across Phase I-III trials.
• Recruitment Expertise: Demonstrated success in accelerating patient recruitment—this is a significant bonus for this role.
• Communication & Personality: A natural "people person" with outstanding communication skills. You are a positive, high-energy team player who thrives in a collaborative startup environment.
• Proven ability of multi-site management, with strong organizational and problem-solving skills
• Discretion: Capable of maintaining the highest level of confidentiality and secrecy regarding sensitive clinical data and company IP.
• Startup Mindset: You are a "do-er" who is comfortable managing the “ins and outs” of clinical operations today while possessing the vision to manage vendors tomorrow.
• Education: B.Sc. or higher in Life Sciences, Pharmacology, or a related field.
• Native-level or excellent written and verbal communication in Hebrew and English.
• Capable of traveling locally and internationally
• Previous experience in Ophthalmology is an advantage
• Availability: This is an immediate opening.

📍 Location: Ramat HaHayal, Tel Aviv (On-site)

Email CV to : [email protected]

Ready to lead the next generation of ophthalmic innovation? Apply now or share this with your network!

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