Senior Vice President of Clinical Operations
2 weeks ago
Key Responsibilities
In this essential position, you will have the chance to influence clinical development across various Therapeutic Areas.
Position Overview
Immix Biopharma is on the lookout for a driven physician executive with a background in drug development to take on the role of Vice President of Clinical Development. This leadership position is part of an expanding clinical development team focused on autoimmune disorders and oncology. You will report directly to the executive leadership and play a crucial role in shaping our portfolio in these therapeutic areas while contributing to the overall clinical development strategy. Your responsibilities will include engaging with clinical sites, contract research organizations (CROs), investigators, and advisory panels. You will also work collaboratively with internal teams, including clinical, translational, and scientific divisions.
This role is strategic, requiring significant interaction with top leadership, while also necessitating hands-on involvement at the program level. You will oversee study execution, program activities, and clinical development plans across the entire portfolio.
The ideal candidate will possess extensive knowledge in both early and late-stage clinical development, along with a proven history of advancing precision therapies from concept to clinical approval, demonstrating strong scientific integrity and a comprehensive understanding of target and disease biology.
- As a pivotal member of the Development Leadership Team, you will provide scientific, clinical, and product development guidance for programs within the Immix Biopharma portfolio.
- Offer indirect leadership to a diverse, cross-functional team of physicians, clinical scientists, and other development professionals.
- Deliver specialized therapeutic area expertise to foster innovation and efficiency in clinical trial design and execution.
- Responsible for the creation and ongoing refinement of clinical development plans for the portfolio from Investigational New Drug (IND) application to Proof of Concept (POC) to New Drug Application (NDA).
- Contribute significantly to IND, NDA, and Premarket Approval (PMA) submissions by overseeing medical documentation and actively participating in discussions with regulatory bodies.
- Serve as the clinical lead for early development studies, including study design, protocol development, regulatory documentation, CRO engagement, study initiation, investigator interactions, data monitoring, regulatory authority communications, analyses, and study reporting.
- Establish and nurture relationships with investigators and thought leaders, closely collaborating with the Medical Affairs team.
- Assist in organizing scientific advisory boards, conference participation, external collaborations, and partnerships.
- Provide medical, disease-specific, and developmental insights into particular research initiatives or broader research programs.
Qualifications
- Medical Doctor (MD/MBBS/DO) degree with fellowship training in rheumatology, medical hematology, or oncology from a US-accredited institution.
- A minimum of three (3) years of clinical development experience within a large pharmaceutical organization.
- In-depth knowledge of autoimmune diseases and oncology, including drug development frameworks, clinical pharmacology, and regulatory approaches.
- Exceptional interpersonal and communication skills, both written and verbal, with the ability to convey complex information clearly and concisely.
- Proven ability to drive collaboration, achieve results, influence stakeholders, and resolve conflicts across various internal and external parties.
- Comprehensive understanding of phase I-IV drug development processes.
- A strong passion for clinical development and precision medicine, with established connections to external experts and credible advisors in the oncology field.
- Demonstrated ability to build and maintain key partnerships and collaborations with the external scientific community, including academia, governmental bodies, nonprofit organizations, and CROs.
Additional Information
- Flexible working arrangements.
- Competitive compensation package, including an annual company bonus.
- Eligibility for stock option grants to acquire shares in Immix Biopharma, Inc.
Your information will be kept confidential in accordance with EEO guidelines.
Immix Biopharma, Inc is dedicated to fostering a diverse workforce that reflects the communities we serve. We believe that diverse and inclusive teams create a stronger and more innovative organization. Therefore, all qualified candidates will be considered for employment without regard to race, religion, color, gender, sexual orientation, age, disability status, marital status, or veteran status.
About Immix Biopharma, Inc.
Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a clinical-stage biopharmaceutical company pioneering cell therapies for AL Amyloidosis and other autoimmune conditions. Our leading cell therapy is the sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201, currently under evaluation in the ongoing Phase 1b/2 NEXICART-1 clinical trial. NXC-201 has the potential to be the world's first "Single-Day CRS" CAR-T, facilitating a quicker return home for patients and supporting further expansion into autoimmune indications. NXC-201 has received Orphan Drug Designation (ODD) from the FDA for both AL Amyloidosis and multiple myeloma, as well as ODD from the European Commission (EMA) for multiple myeloma and AL Amyloidosis. Learn more at our website.
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