To Discuss more about this job opportunity, please reach out to Deepak Arya LinkedIn URL www.linkedin.com/in/deepak-arya-8a79aa22a email your updated resume at Email deepak.arya@collabera.com Thank you!

Pay Range: $100 to $120 an hour (Negotiable based on the experience)

Industry: Pharmaceutical

Job Mode: 100% Remote

Contract Duration: 06 Months (Possibility of Extension)

Job Summary:
We are seeking an experienced Medical Director to lead clinical development activities within oncology programs in a large enterprise environment. This role involves designing and overseeing clinical trials, ensuring high quality data interpretation, and maintaining compliance with regulatory standards. The ideal candidate will bring deep therapeutic expertise in lymphoma and immunotherapy along with strong leadership in clinical trial execution. You will collaborate across global teams and contribute to strategic development decisions. This position requires strong scientific judgment and the ability to manage complex clinical programs in a fast paced environment.

Key Responsibilities:

• Manage the design implementation and evaluation of clinical study protocols aligned with the product development strategy.
• Provide oversight of clinical trials including monitoring study integrity and reviewing safety and efficacy data.
• Collaborate with clinical operations to oversee enrollment timelines and key deliverables.
• Review and report serious adverse events in compliance with regulatory and corporate standards.
• Lead training and education initiatives for investigators and study personnel.
• Ensure adherence to Good Clinical Practice pharmacovigilance and quality standards.
• Work closely with cross functional teams including clinical development regulatory safety and quality.
• Communicate clinical insights and findings effectively to internal and external stakeholders.
• Support continuous quality improvement activities including audits and peer reviews.
• Provide updates and strategic input to senior leadership on clinical and operational matters.

Required Qualifications:

• Medical Doctor or equivalent degree with relevant clinical specialization
• US residency training
• Minimum 5 years of clinical or clinical development experience
• Strong experience in medical monitoring and clinical trials
• Ability to interpret safety and efficacy data independently
• Experience working in global clinical environments

Preferred Qualifications:

• Experience in lymphoma clinical trials or lymphoma patient care
• Experience with immunotherapy program
• Prior experience in pharmaceutical or biotech clinical development
• Fellowship training in a relevant subspecialty
• Strong understanding of regulatory and compliance frameworks

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401 k retirement plan, life insurance, long term disability insurance, short term disability insurance, paid parking public transportation, paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually AS Applicable