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 global clinical trials that facilitate product registration and commercialization.

• Execute global clinical trials while ensuring patient safety and managing adverse-event follow-up.

• Assess protocols, study reports, publications, labeling, pricing, reimbursement, access documents, grants, and contracts.

• Act as a scientific resource for study teams, departments, clinical operations personnel, investigators, and ethics committees.

• Collaborate on clinical strategy, lifecycle plans, development plans, and the design of study protocols.

• Design, implement, and report on local clinical trials, while aiding in study start-up, investigator training, and site activities.

• Evaluate investigator-initiated trial proposals and associated publications.

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

• Assist with symposia, advisory boards, congresses, medical information responses, data analyses, slide presentations, abstracts, posters, and manuscripts.

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

• Provide medical expertise for regulatory reports, label modifications, advisory committees, risk management, and registration initiatives.

• Contribute to medical strategies, brand commercialization, payer partnership programs, product value defense, and strategic brand planning.

• Aid in the development of promotional materials and define the patient journey and key moments of truth.

• Assess medical literature, competitive products, clinical practice trends, and access developments.

• Deliver scientific training and protocol expertise to clinical study teams.

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

• Collaborate with alliance, business, and vendor partners while exemplifying Lilly leadership behaviors.

⛳️ Requirements

• Medical Doctor degree required.

• Board eligible or certified in an appropriate specialty/subspecialty, or possess comparable post-medical-school clinical training relevant to the hiring country.

• US-trained physicians must attain board eligibility or certification.

• Non-US-trained physicians must have graduated from a medical school that meets LCME requirements.

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

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

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

• Adherence to applicable local and international regulations, laws, guidelines, Good Clinical Practices, company standards, policies, procedures, and integrity agreements.

• Maintain necessary qualifications and training, including a current curriculum training map.

🏝️ Benefits

• Company bonus based on both company and individual performance.

• Participation in a 401(k) plan.

• Pension plan benefits.

• Vacation benefits.

• Medical coverage.

• Dental coverage.

• Vision coverage.

• Prescription drug coverage.

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

• Life insurance and death benefits.

• Time off and leave of absence benefits.

• Well-being benefits, including employee assistance programs, fitness benefits, and employee clubs and activities.

• Employee resource groups that are open to all employees.