We are recruiting medical professionals for a specialized clinical environment conducting human studies for cosmetic testing, within a structured, procedure-driven setting and international standards.

This opportunity is open to:

• Senior dermatologists / specialists
• Residents (Dermatology)
• General practitioners (Medical doctors)
• International doctors with valid right to practice in Romania (drept de liberă practică)

You will coordinate the medical component of cosmetic studies, support ethics submissions and sponsor communication, and supervise study-team execution in line with applicable procedures and the study protocol.

Key Responsibilities 

• Coordinates and leads the technical conducting for clinical study in accordance with the main Investigator’s instructions;
• Establishes the inclusion and exclusion criteria necessary for conducting the clinical study and communicates them to the study documentation and/or recruitment department personnel at the Investigator’s request;
• Participates in the evaluation of the study request/protocol;
• Provides the necessary information about the study project to the Internal Ethics Committee, External Ethics Committee, or IRB (Institutional Review Board) for evaluation;
• Prepares/verifies/approves/complies with/applies/transmits to the Sponsor the protocol and/or its amendments as a support for documentation department;
• Approves and signs the study report, ICF (informed consent form), CRF (Case Report Form) and all component documents of the ISF (investigational study file) according to current procedures;
• Protects the rights, safety, and comfort of study participants;
• Includes subjects in the study by verifying clinical inclusion criteria,
• Ensures the follow-up of the subjects involved in an adverse event as long as necessary;
• Ensures that during the clinical study, the study team under their supervision complies with the assigned responsibilities;
• Documents and informs the Internal Ethics Committee, External Ethics Committee, or IRB (Institutional Review Board) of any protocol deviations, adverse events, and/or significant adverse events;
• Records and secures source data in both electronic and paper formats;
• Verifies and re-verifies source data recorded by technical department employees in source documents;
• Makes corrections and/or implements necessary corrective actions and/or requests corrections in source documents within the clinical study process;
• Notifies the Sponsor or their designated persons about adverse events according to the study protocol and current procedures at the Investigator’s request;
• Clinically examines each potential subject during the subject recruitment process; creating a brief history regarding personal physiological, pathological, hereditary, and treatment history, and a questionnaire regarding cosmetic habits;
• Verifies the health status of each subject in accordance with the notion of “healthy subject” as defined in the company’s “General Conditions for Conducting Human Tests”;
  

Benefits

• International working environment
• Opportunity to collaborate with very known brands
• Private medical insurance
• Meal vouchers
• Performance bonuses
• Transportation subscription / support
• Clear procedures, training, and a stable, professional medical framework

All candidates who meet the above qualifications are warmly encouraged to submit their applications online. We will reach out exclusively to those who are best suited for the role within a maximum of two weeks.

For other job opportunities, visit our website at www.puntoup.com and upload your CV to our database to remain eligible for both current and future positions. All applications are handled with the utmost confidentiality.

By submitting your personal data via email to any address ending in “www.puntoup.com” or “www.puntoup.ro,” through social media platforms (such as Facebook, LinkedIn), or by applying via an online job portal, you provide explicit consent for PuntoUP and its affiliated companies to process your data. For more information, please refer to our data processing policy. Should you have any concerns regarding your personal data, kindly contact dataprotection@puntoup.com.