Licensed Physician/Specialist, Clinical Research

Humaneva Group

. Perform physician duties as an investigator in accordance with applicable pharmaceutical and medical device legislation .

Posted 10/22/2026full-timeBerlin • GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting clinical trials, including obtaining informed consent, validating participant information, and adhering to Good Clinical Practice (GCP) regulations. Possesses strong communication skills in both German and English, with a commitment to collaboration and professionalism in interactions with study participants and partners.

Highest-signal resume keywords

Medical LicenseClinical Trials ExperienceGood Clinical Practice (GCP)Excellent Written and Spoken GermanUniversity Degree

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Conducting Medical ExaminationsObtaining Informed ConsentData Collection and DocumentationImplementing Study ProtocolsRisk Identification and Management

Soft Skills

Team-OrientedMotivatedFriendly MannerStrong Collaborative Skills

Certifications & Qualifications

Specialist Certification in General MedicineSpecialist Certification in Internal MedicineSpecialist Certification in Oncology

Industry Keywords

Pharmaceutical LegislationMedical Device LegislationStudy Participant InteractionTraining SessionsInternational Collaboration

About the role

Key responsibilities & impact

Perform physician duties as an investigator in accordance with applicable pharmaceutical and medical device legislation
Take medical histories, conduct examinations, and provide information to study participants
Obtain informed consent from study participants
Validate study participants’ self-reported information
Implement study and examination protocols
Conduct studies involving patients
Identify risks and initiate necessary measures
Collect and document study-related data
Prepare for, support, and participate in training sessions and certifications
Collaborate with regional, national, and international partners

Requirements

What you’ll need

Medical license to practice as a physician (m/f/d) or specialist certification (m/f/d) in general medicine, internal medicine, oncology, or another medical specialty
Experience planning, organizing, and conducting clinical trials is an advantage
Knowledge of applicable regulations, including Good Clinical Practice (GCP), is an advantage
Team-oriented, committed, and motivated
Friendly and professional manner when interacting with study participants, team members, and external partners
Excellent written and spoken German
Good English skills are an advantage
Strong collaborative skills
University degree; must be submitted during the application process

Benefits

Comp & perks

Exciting, varied, and responsible role with opportunities for professional and personal growth
Open and transparent communication in a modern company with flat hierarchies
Support for personal and professional development
Opportunity to help shape workflows and processes
Flexible working hours by agreement
Professional network with teams in other cities across Germany and throughout Europe
Diverse career development opportunities in Germany and across Europe
30 days of annual leave
Company-funded professional training and the necessary resources
Complimentary beverages
Monthly team meals
Team-building activities and team events