Head of Compliance Operations - Boston, MA, United States - EPM Scientific - Phaidon International

Description

Director, Clinical Operations
$The biotechnology company is at the forefront of groundbreaking research in the field of Immuno-Oncology. They harness the power of the immune system to fight cancer, firmly establishing themselves as pioneers in this rapidly evolving field. Guided by a visionary team of industry veterans and seasoned experts, their leaderships paves the way for unparalleled success and growth within the biotech industry. Their proven track record in oncology speaks for itself. They've developed innovative gene therapies that have shown remarkable efficacy in targeting cancer cells with unprecedented precision, offering new hope to patients and transforming the landscape of cancer care. With their expertise in gene therapy and commitment to scientific innovation, they've poised to extend the reach of our technology to tackle other therapeutic challenges. Leveraging their cutting-edge gene therapy platform io address a broader spectrum of diseases in other therapeutic areas.

As the Director of Clinical Operation, you will play a key role in leading and overseeing clinical operations activities for their Immuno-Oncology programs.

Based in their Boston office, you will be responsible for driving the successful execution of clinical trials from early-phase trials through phase III.

The Director will guide the planning and management of these programs, making sure everything runs smoothly.

This is a dynamic leadership position within a cutting-edge biotech company dedicated to revolutionizing different treatments with gene therapy .

Offers strategic leadership, expert guidance, and thorough oversight to ensure the seamless management of all clinical trials.
Designs, implements, and meticulously manages clinical trials within allocated budgets and predetermined timelines.
Identifies, evaluates, and selects suitable investigators/sites and service providers in alignment with project needs and company standards.
Leads and mentors a dynamic clinical team, fostering individual career growth and monitoring professional advancement.

Facilitates cross-departmental collaboration with research and development, regulatory affairs, and medical affairs to drive comprehensive trial strategies and execution.

Will only consider candidates with recent experience within a biotech/ pharma company.
Requires a minimum of 5 years of experience in senior management roles within the industry.
Must hold an advanced agree in relevant scientific discipline.

Extensive experience leading and managing the end-to-end interview process as a hiring manager, ensuring the successful identification and selection of top talent.

Demonstrated track record of effectively managing clinical studies within designated program budgets and timelines, including expertise in developing clinical study protocols, regulatory documentation, and SOPs.

Note:
This is a confidential search. All inquiries and applications will be handled with discretion
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