Clinical Research Physician – Malignant Hematology

This is a fully remote position, open to applicants in United States.

📋 Description

• Engage in the development, execution, and reporting of corporate/global clinical trials that facilitate product registration and commercialization.

• Execute global clinical trials while ensuring patient safety, which includes monitoring adverse events and follow-up procedures.

• Assess protocols, informed consent documents, study reports, publications, labels, regulatory submissions, and various scientific materials.

• Collaborate on clinical strategies, lifecycle plans, development frameworks, value propositions, and the design of study protocols.

• Aid in the design, execution, reporting, initiation, investigator selection, and training of site personnel for clinical trials.

• Act as a scientific resource for clinical operations staff, investigators, ethical review boards, and study teams.

• Address the scientific information needs of investigators, healthcare professionals, payers, patients, and other stakeholders.

• Assist in data analysis, dissemination of scientific data, organization of symposia, advisory boards, congresses, slide presentations, abstracts, posters, manuscripts, and final reports.

• Build and sustain relationships with external experts, thought leaders, professional societies, investigators, and the broader medical community.

• Provide medical expertise for regulatory reports, label modifications, FDA interactions, advisory committees, and risk management planning.

• Contribute medical and scientific knowledge to commercialization efforts, payer partnership initiatives, promotional materials, patient journey mapping, and brand strategies.

• Deliver scientific training and serve as a protocol expert and consultant for clinical study teams.

• Support development budgets, professional growth, recruitment, diversity, retention efforts, committees, Six Sigma initiatives, and task forces.

⛳️ Requirements

• Medical Doctor.

• Board eligible or certified in the relevant specialty/subspecialty, or have completed comparable post-medical-school clinical training pertinent to the hiring country.

• Physicians trained in the US must achieve board eligibility or certification.

• Non-US-trained physicians must have completed their education and training at a medical school that meets LCME standards.

• A minimum of 3 years of industry experience in oncology or malignant hematology is preferred.

• Proven experience and understanding of clinical research and the pharmaceutical development process.

• Exceptional communication, interpersonal, organizational, teamwork, and negotiation abilities.

• Knowledge of and adherence to relevant local and international regulations, laws, guidelines, Good Clinical Practices, company standards, policies, and procedures.

• Capability to critically assess medical literature and stay abreast of developments in clinical, scientific, competitive-product, and clinical-practice fields.

• Ability to provide scientific training and act as a protocol expert for clinical study teams.

• Proficiency in collaborating with clinical, regulatory, legal, marketing, patient safety, business, and vendor partners.

• Capacity to maintain current training and curriculum documentation as required.

🏝️ Benefits

• Company bonus eligibility based on both company and individual performance.

• Company-sponsored 401(k).

• Pension plan.

• Vacation benefits.

• Medical coverage.

• Dental coverage.

• Vision coverage.

• Prescription drug benefits.

• Flexible benefits, including healthcare and/or dependent daycare flexible spending accounts.

• Life insurance and death benefits.

• Specific time off and leave of absence benefits.

• Well-being perks, which include an employee assistance program and fitness benefits.

• Employee clubs and activities.

• Employee resource groups providing support networks.

• Accommodation support for individuals with disabilities during the application process.