What is the salary for this Sr. Medical Director/VP, Clinical Development role?

Salary information is not publicly listed for this position. Apply directly to discuss compensation with Kelonia Therapeutics.

Where is this Sr. Medical Director/VP, Clinical Development position located?

This is an on-site position at Kelonia Therapeutics located in Boston, MA.

How do I apply for this Sr. Medical Director/VP, Clinical Development job at Kelonia Therapeutics?

Click the 'Apply' button on this page to be redirected to Kelonia Therapeutics's application portal. Make sure to have your resume ready and tailor your application to highlight relevant experience.

What is Kelonia Therapeutics?

Kelonia Therapeutics is actively hiring for Healthcare roles. Visit the company page to see all open positions and learn more about working at Kelonia Therapeutics.

Sr. Medical Director/VP, Clinical Development

Kelonia Therapeutics Boston, MA Today

healthcare

Here at Kelonia Therapeutics, we aren’t just a clinical company; we’re trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. We're not just a team; we're dreamers on a mission to bring the promise of cell and gene therapy to every patient in need.

We've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart. We're not just building a company; we're cultivating a culture that values both skill and care.

Are you ready to be a part of our remarkable journey? We're looking for someone exceptional to join our growing team as a Sr. Medical Director/VP in the Clinical Development group to provide medical and strategic leadership from IND through clinical proof-of-concept and beyond. In this role, you will guide and support clinical programs, oversee the day-to-day medical monitoring, clinical development, data services, and pharmacovigilance for lead programs, as well as future indications. This isn't just a job; it's an opportunity to contribute to groundbreaking therapies, be at the forefront of advancing our oncology programs, and to make a transformative impact on patients' lives. Join us at the forefront of innovation and help write the next chapter in gene therapy.

What You will Do:

Provide medical and scientific leadership for the company’s oncology programs, ensuring alignment with clinical development goals.

Collaborate with cross-functional teams (R&D, regulatory, clinical operations, translational science, and biometrics) to develop and implement translational strategies that bridge preclinical discoveries to clinical applications.

Lead the design, review, and oversight of clinical to evaluate drug candidates' efficacy, safety, and pharmacodynamics.

Contribute to regulatory filings (e.g., IND submissions) by providing scientific and medical expertise, ensuring the successful progression from preclinical to clinical stages.

Analyze and interpret clinical and correlative data to support decision-on program advancement.

Build and maintain relationships with external KOLs, academic institutions, and clinical trial sites to support future clinical trial design and execution.

Provide clinical insights on drug development, including patient selection strategies, safety considerations, and efficacy assessments.

Contribute to the company’s overall strategy by identifying emerging trends and opportunities within the biotech landscape.

What You will Bring:

MD required with expertise in oncology, hematology, or a related field.

3+ years of experience in oncology drug development, including early-stage clinical trials in biotech or pharma.

Required experience CAR-T, advanced oncology modalities such as immunotherapies, or gene therapy.

Prior experience with IND filings and regulatory submissions (preferred).

Strong understanding of tumor biology, immuno-oncology, and targeted therapies.

Expertise in translational research and regulatory requirements for advancing compounds from preclinical to clinical development.

Ability to analyze complex scientific data and communicate findings effectively to both technical and non-technical stakeholders.

Regulatory experience, including FDA/EMA interactions highly preferred.

Established network with KOLs and clinical investigators in oncology.

Strong leadership, collaboration, and problem-solving skills in a fast-paced biotech environment.

At Kelonia, we’re serious about balance and growth. You’ll get Flexible Time Off, flexible scheduling that aligns with your needs and our objectives, a competitive benefits package (health, commuter, and more), and great on-site perks that include free parking, a state-of-the-art gym, and a food hall – all within a collaborative, inclusive team that invests in your development and makes big things happen together.

Kelonia Therapeutics is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Kelonia does not accept unsolicited resumes from any source other than directly from candidates.

Job Type: Full-time

Work Type: Flexible

Location: Boston, MA