Medical Director(Hematology/Oncology) - Remote U.S

Lensa; Greenville (NC); Remote; USD 200,000 - 300,000; Full time

Job summary

A leading company is seeking a Medical Director specializing in Hematology/Oncology to oversee clinical trials and ensure compliance with regulations. This remote role involves providing medical consultations, managing safety data, and supporting business development. Ideal candidates will have an MD, clinical experience, and strong communication skills. Competitive pay and benefits are offered.

Benefits

Competitive pay

Bonuses

Healthcare

Career development opportunities

Qualifications

• Clinical experience in treating patients and industry experience in clinical trials or safety/pharmacovigilance.
• Knowledge of therapeutic areas, safety databases, and regulations (FDA, ICH, EMA, GCP).

Responsibilities

• Ensure proper execution of tasks related to pharmacovigilance, adhering to regulations and SOPs.
• Provide medical consultation and communicate effectively with team members and clients.
• Monitor safety variables during clinical studies and discuss medical concerns with investigators and clients.

Skills

Decision-Making

Communication

Organizational

Analytical

Flexibility

Independence

Education

MD or equivalent with specialization in Oncology or Hemato-Oncology

Job description

Medical Director(Hematology/Oncology) - Remote U.S

Lensa is the leading career site for job seekers at every stage of their career. Our client, Thermo Fisher Scientific, is seeking professionals. Apply via Lensa today!

Work Schedule: Standard (Mon-Fri)

Environmental Conditions: Office

Job Description: As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information: Our Pharmacovigilance team manages the safety profile of new drugs in clinical trials, oversees case-processing activities, and performs regulatory reporting and medical monitoring. This role involves managing clinical trials through all stages of drug development, including oversight of contracted services.

Discover Impactful Work: The Medical Director provides medical oversight of clinical trials, ensuring compliance with SOPs, client directives, GCP, and regulatory requirements. Responsibilities include attending investigator and sponsor meetings, providing medical consultations, supporting business development, and reviewing safety data and reports.

Key Responsibilities:

• Ensure proper execution of tasks related to pharmacovigilance, adhering to regulations and SOPs.
• Provide medical consultation and communicate effectively with team members and clients.
• Contribute to writing and reviewing clinical safety and efficacy reports.
• Monitor safety variables during clinical studies and discuss medical concerns with investigators and clients.
• Review adverse events and perform data validation to assess safety concerns.
• Manage signal detection activities, review safety reports, and support dossier maintenance.

Qualifications:

• MD or equivalent with specialization in Oncology or Hemato-Oncology; active medical license preferred.
• Clinical experience in treating patients and industry experience in clinical trials or safety/pharmacovigilance.
• Knowledge of therapeutic areas, safety databases, and regulations (FDA, ICH, EMA, GCP).

Skills and Abilities:

• Strong decision-making, communication, organizational, and analytical skills.
• Flexibility to travel domestically and internationally.
• Proficiency in computer applications and fluent in English.
• Ability to work independently, mentor others, and handle complex information under stress.

Physical Requirements: Office environment with occasional travel, standing, mobility, and light lifting.

Benefits: Competitive pay, bonuses, healthcare, and career development opportunities. Thermo Fisher Scientific is an equal opportunity employer.