Clinical Operations Manager - REMOTE

Jobgether

3d • Remote

About The Position

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Operations Manager - REMOTE. In this pivotal role, you will be at the forefront of advancing healthcare innovation, focusing on ophthalmology and related fields. You will drive the planning, execution, and oversight of clinical research protocols, ensuring alignment with regulatory and business objectives. Your leadership will help establish a new Clinical Affairs function and enhance the quality of life for patients globally through groundbreaking therapies. Collaboration with cross-functional teams will be essential as you contribute significantly to our mission. This role offers the opportunity to impact patient care while working in a flexible remote setting, with occasional travel required.

Requirements

• Degree in life sciences, with a specialization in ophthalmology strongly preferred.
• Minimum 7 years’ experience in clinical operations, including direct oversight of CROs.
• Demonstrated experience in project managing clinical trials.
• Experience in ophthalmology preferred.
• Excellent communication, stakeholder engagement, and cross-functional collaboration skills.
• Self-starter with strong initiative and ability to work independently.
• Experience in regulatory compliance and clinical documentation.
• Fluent in English.

Nice To Haves

• Experience in ophthalmology preferred.
• Degree in life sciences, with a specialization in ophthalmology strongly preferred.

Responsibilities

• Lead the operational planning and execution of clinical studies, ensuring alignment with regulatory and business objectives.
• Manage relationships with CROs, vendors, and external partners to ensure high-quality, timely, and cost-effective study delivery.
• Project manage clinical trials, overseeing timelines, budgets, and deliverables.
• Provide regular updates and insights to core project teams, ensuring effective communication and alignment across functions.
• Support the coordination and submission of scientific publications.
• Ensure compliance with GLP, GCP, and all regulatory standards, documenting all research activities and findings.
• Proactively identify and mitigate risks in clinical development.
• Report study progress and outcomes to internal and external stakeholders and contribute to regulatory dossier preparation.

Benefits

• Opportunity to work remotely with approximately 20% travel required.
• Be a part of a team that is at the forefront of healthcare innovation.
• Contribute to the development of groundbreaking therapies and solutions.
• Equal employment opportunities and a commitment to diversity and inclusion.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager