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 • CroatiaLeadWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in medical monitoring, clinical trial oversight, and pharmacovigilance, with a strong foundation in clinical medicine and extensive experience in managing Phase I-IV studies. 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 OversightPharmacovigilanceFDA, EMA, And ICH-GCP GuidelinesMedical Data Review

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Medical MonitoringClinical DevelopmentSafety ManagementRisk ManagementProtocol ReviewStudy DesignEndpoint DevelopmentAdverse Event IdentificationStatistical Analysis Plans ReviewClinical Study Reports Review

Soft Skills

LeadershipOrganizational SkillsCommunication SkillsInterpersonal SkillsTeamwork

Tools & Technologies

Centralized TrackerCTMSMedDRAWHODrug

Certifications & Qualifications

Advanced Certification In HematologyAdvanced Certification In Oncology

Industry Keywords

Clinical TrialsContract Research OrganizationGlobal Clinical TrialsMulti-Regional Study TeamsSafety Oversight

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 study sites
Answer site questions about eligibility and enrollment
Perform safety and patient management
Advise on medical questions and issues arising during clinical trials
Define, plan, and provide medical monitoring for assigned clinical trials with cross-functional teams and sponsors
Develop Medical Monitoring Plans and Safety Management Plans
Review protocols and protocol training materials
Train project teams on disease areas, study design, and procedures
Attend and participate in Investigator Meetings when applicable
Consult on inclusion/exclusion criteria 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, serious adverse events, medical history, and concomitant medications
Identify safety concerns, adverse events, risks, trends, and safety signals and develop appropriate responses
Consult on out-of-range laboratory values for clinical and protocol significance
Advise Pharmacovigilance/Drug Safety on SAE assessment and reporting
Review subject narratives, periodic and interim safety reports, and other 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 Standard Operating Procedures 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 is highly preferred
Proven experience managing clinical trials in a Contract Research Organization or pharmaceutical company environment
Expertise in Phase I-IV studies
In-depth knowledge of FDA, EMA, and ICH-GCP 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 risk management in clinical trials
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-focused, and quality-focused

Benefits

Comp & perks

Remote work arrangement
Equal opportunity employment
Recruitment and selection accommodations for candidates with disabilities upon request