Medical Monitor / Director

• Lymphoma trial experience and/or clinical experience in lymphoma
• Medical monitoring and/or clinical experience with immunotherapies
• MD with U.S. residency training (preferred)
• Ability to work with global sites across multiple time zones
• Strong capability to independently interpret safety and efficacy data and proactively identify/escalate risks

Key Responsibilities

• Manage the design, implementation, and evaluation of clinical study protocols aligned with the overall Product Development Plan
• Provide oversight of clinical studies, ensuring study integrity and reviewing safety and efficacy data
• Collaborate with Clinical Operations to manage enrollment, timelines, and key deliverables
• Assess and report serious adverse events in compliance with regulatory requirements and company policies
• Lead education and training initiatives for investigators, site personnel, and internal teams
• Maintain up-to-date expertise in the therapeutic area through literature and continuous learning
• Ensure compliance with Good Clinical Practice (GCP), pharmacovigilance standards, SOPs, and regulatory requirements
• Uphold the highest standards of medical ethics and seek consultation when required
• Collaborate cross-functionally with Clinical Development, Medical Affairs, Regulatory, Safety, and Quality teams
• Communicate scientific and clinical findings clearly to internal and external stakeholders
• Participate in quality assurance activities, audits, and continuous improvement initiatives
• Provide updates to senior leadership on clinical and operational matters
• Support training and knowledge sharing within the Clinical Development team
• Represent the organization in meetings, committees, and review boards as required

Qualifications

• MD, DO, or international equivalent with relevant therapeutic specialty experience
• U.S. residency training strongly preferred; subspecialty fellowship is a plus
• 5+ years of experience; lymphoma clinical or trial experience preferred
• Medical monitoring experience, especially with immunotherapies, is highly desirable
• Clinical trial experience in pharma, academia, or equivalent setting
• Strong understanding of clinical trial methodology, study oversight, and regulatory requirements
• Ability to collaborate effectively in a cross-functional, matrixed environment
• Experience working with global teams across multiple time zones

Core Competencies

• Strong analytical and clinical judgment
• Ability to interpret safety and efficacy data and escalate risks appropriately
• Excellent communication and stakeholder management skills
• High attention to detail and organizational skills
• Ability to manage multiple priorities in a fast-paced environment
• Knowledge of GCP, pharmacovigilance, and clinical research compliance

SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at nahr@spectraforce.com if you require reasonable accommodation.