Medical Director, Oncology

Everest Clinical Research

. Work with business development and internal stakeholders to critically appraise protocols, propose study designs, and develop endpoints .

Posted 10/30/2026full-timeRemote • RomaniaLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical monitoring, clinical trial oversight, and pharmacovigilance, with a strong foundation in clinical medicine and extensive experience in managing clinical trials. Proficient in regulatory compliance and safety management, with the ability to collaborate effectively across cross-functional teams.

Highest-signal resume keywords

Doctor Of Medicine (MD)Clinical Trial OversightPharmacovigilanceMedical MonitoringRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical DevelopmentMedical Data ReviewSafety OversightRisk ManagementProtocol ReviewStudy DesignAdverse Event IdentificationStatistical Analysis PlansSAE AssessmentClinical Study Reports

Soft Skills

LeadershipOrganizational SkillsCommunication SkillsInterpersonal SkillsTeamwork

Tools & Technologies

CTMSMedDRAWHODrug

Certifications & Qualifications

Advanced Certification In HematologyAdvanced Certification In Oncology

Industry Keywords

FDA RegulationsEMA GuidelinesICH-GCPPhase I–IV StudiesClinical TrialsCRO EnvironmentGlobal Clinical Trials

About the role

Key responsibilities & impact

Work with business development and internal stakeholders to critically appraise protocols, propose study designs, and develop endpoints
Serve as primary medical monitor and first point of contact for clinical trial sites
Answer site questions regarding eligibility and enrollment, and perform safety and patient management
Advise on medical questions and issues arising during clinical trials
Define, plan, and provide medical monitoring for assigned trials with cross-functional teams and sponsors
Contribute medical expertise to Medical Monitoring Plans and Safety Management Plans
Review protocols and protocol training materials
Train project teams on disease or therapeutic areas, study design, and procedures
Attend and participate in Investigator Meetings when applicable
Support decisions on inclusion/exclusion deviations and protocol-related questions
Respond to medical queries from Investigators, Ethics Committees, and Data Monitoring Committees
Provide emergency medical guidance outside normal business hours by telephone and email
Document protocol inquiries and answers in the centralized tracker/CTMS
Review listings, laboratory reports, subject profiles, safety data, SAEs, medical histories, and concomitant medications
Identify safety concerns and adverse events and develop and execute appropriate responses
Consult on out-of-range laboratory values for clinical and protocol significance
Advise Pharmacovigilance/Drug Safety on SAE assessment and reporting queries
Review subject narratives, periodic and interim safety reports, and study documentation
Assist with medical review of MedDRA and WHODrug-coded terms
Review Statistical Analysis Plans, tables, figures, listings, and Clinical Study Reports as needed
Ensure compliance with company SOPs and clinical-trial safety medical-monitoring practices

Requirements

What you’ll need

Doctor of Medicine (MD) from an accredited institution
Strong foundation in clinical medicine
Practical experience in medical research or clinical development
At least 10–15 years of experience in clinical development
Strong background in medical monitoring, clinical trial oversight, and pharmacovigilance
Advanced certification, specialization, or therapeutic-area expertise in hematology, oncology, or another relevant medical field highly preferred
Proven experience managing clinical trials in a CRO or pharmaceutical company environment
Expertise in Phase I–IV studies
In-depth knowledge of FDA, EMA, and ICH-GCP regulatory requirements and guidelines
Strong leadership, organizational, and communication skills
Ability to work collaboratively in cross-functional teams and interact effectively with internal and external stakeholders
Expertise in medical data review, safety oversight, and clinical-trial risk management
High attention to detail and ability to make informed decisions based on clinical data
Ability to maintain confidentiality and handle sensitive medical and client data responsibly
Experience working with global clinical trials and multi-regional study teams
Excellent interpersonal and teamwork skills; detail-oriented, customer- and quality-focused

Benefits

Comp & perks

Equal opportunity and disability accommodations available upon request
Remote work arrangement