Cellectis

19 Cellectis Jobs Hiring Near You

Cellectis Department: Clinical Development Position Summary Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company's medical affairs ...

Warehouse Associate / Kitter II

Raleigh, NC

$15.50 - $18.50/hr

Schedules with couriers Cellectis cGMP material shipments to clinics and samples to contract laboratories * Executes basic mechanical activities related to maneuvering cryogenic (liquid nitrogen ...

Warehouse Associate / Kitter II

Raleigh, NC

$15.50 - $18.50/hr

Schedules with couriers Cellectis cGMP material shipments to clinics and samples to contract laboratories * Executes basic mechanical activities related to maneuvering cryogenic (liquid nitrogen ...

Warehouse Associate / Kitter II

Raleigh, NC ยท On-site

$15.50 - $18.50/hr

Schedules with couriers Cellectis cGMP material shipments to clinics and samples to contract laboratories * Executes basic mechanical activities related to maneuvering cryogenic (liquid nitrogen ...

Director, Clinical Quality Assurance

Raleigh, NC ยท On-site

$190K - $2.34M/yr

This position is also part of the Global Cellectis Quality Leadership team actively contributing to the overall global Quality strategy and initiatives. Position Responsibilities * Defines and ...

This role is responsible for the execution, accountability, and ownership of Metrology activities at the Cellectis, Raleigh, NC facility. Responsible for maintaining an audit ready metrology program ...

The Senior Director Biostatistics will partner with other company leaders to design and implement clinical development plans, and overall development strategy for Cellectis' programs and products.

Clinical Trial Associate

Manhattan, NY ยท On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Position Responsibilities * Assist in responding to site during normal business hours and potentially off-hours and weekends to maintain operations as needed. * Manage equipment reliability ...

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing ...

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing ...

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Position Responsibilities * Assist in responding to site during normal business hours and potentially off-hours and weekends to maintain operations as needed. * Manage equipment reliability ...

Cellectis Jobs Information

What are the most popular states for Cellectis jobs?
Infographic showing various job openings at Cellectis in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.

Senior Director, Medical Affairs

Cellectis

Manhattan, NY โ€ข On-site

$175/hr

Full-time

Posted 11 days ago


Job description

Job Description
Location: New York, NY (Hybrid)
Company: Cellectis
Department: Clinical Development
Position Summary
Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company's medical affairs strategy across its clinical-stage portfolio. Reporting to the Chief Medical Officer, this leader will elevate Cellectis' scientific presence, support pipeline advancement, and ensure medical excellence in evidence generation, scientific communications, and external engagement.
This role is ideal for a medical affairs leader with strong immuno-oncology expertise, strategic agility, and a passion for patient-centered innovation.
Key Responsibilities
  • Partner with the CMO to develop and execute Cellectis' medical affairs strategy.
  • Build and manage critical medical affairs capabilities, including medical strategy, medical communications, publications, and scientific engagement.
  • Provide expert scientific and medical insights across immuno-oncology programs.
  • Lead engagement with key opinion leaders, investigators, and scientific experts.
  • Represent Cellectis at scientific meetings, advisory boards, and congresses.
  • Drive creation of scientific platforms and data-driven communication strategies.
  • Oversee development of medical information, publications, and internal scientific education.
  • Identify and address data gaps through evidence-generation initiatives.
  • Support clinical development and early-access programs with medical expertise.
  • Integrate patient insights into medical and clinical strategies.
  • Partner cross-functionally with clinical development, regulatory and communications affairs to ensure alignment and shared decision-making.
  • Establish governance processes, operational metrics, and reporting frameworks.
  • Promote a culture of scientific rigor, compliance, and patient focus.

Education and Experience
  • Pharm D or MD experience in Hematology / Oncology --
  • 15+ years of medical affairs and/or clinical development experience in the biopharmaceutical industry.
  • Demonstrated experience engaging KOLs, TA experts, payors and patient advocacy organizations.
  • Experience in drug development and/or clinical practice; demonstrated knowledge of competitive landscape, trends, and physician practices.
  • Skilled at presenting clinical and non-clinical data to external audiences and management team(s)
  • Clinical development experience highly preferred.

Core Competencies
  • Excellent clinical judgment and decision-making skills.
  • Strong interpersonal and communication skills, with the ability to influence cross-functional teams.
  • Demonstrated ability to build strong partnerships with investigators, KOLs, and internal stakeholders.
  • Proven ability to lead cross-functional teams in a matrixed environment.
  • Mission-driven leader with a passion for improving patient outcomes.
  • Comfortable in a fast-paced, innovative biotech environment.
  • Ability to travel up to 50-60% of time

Compensation Range: $175-225k