We are searching for our client, a non-corporate pharmaceutical company, a motivated candidate for the Medical Advisor role. On this position you will manage and supervise the worldwide clinical and postmarketing trials, you will be responsible for medical monitoring, you will work on analyzing and publishing quality clinical data for new as well as existing products with aim of achieving regulatory approvals and KOL support.

This role is suitable for junior candidates/ Medical Doctors with 2 - 7 years of experience in hospital, clinical research, R&D, PV or medical advisory.

Main Responsibilities:

* Medical Advisor for an indication /or group of indications for a compound in development in gynecology

* Efficient and safe development of the compound in indication(s) assigned, including competent medical monitoring of individual clinical & postmarketing trials

* Medical representation of the company

* Medical monitoring of trials, with focus on medical review of study documentation and individual patient information, investigator communication, and together with vigilance continuous safety evaluation

* Author, and/or support writing, and/or reviewing of medical documents; such as clinical study protocols, investigator's brochures, clinical study reports, clinical development plans, internal and external presentations etc.

* Support development of case report forms, statistical analysis and other related documents

* Close interaction across the whole development team to support efficient and safe conduct of clinical & postmarketing studies

* Close interaction with Regulatory Affairs

* Establish and maintain close interaction with investigators within the appropriate area of work to secure support for the clinical program

* Participate in preparation of Advisory Boards and Investigator´s Meetings.

We require:

Professional Experience and Qualifications

* Medical doctor degree (is a must)

* Medical devices or drug development industry experience min. 2 years, if not: clinical research or pharmacovigilance experience

* Ability to interact with different professional levels of the research community

* Knowledge of ethical principles and drug or medical device laws and regulations

* Fluent Czech and very good English

* Strong computer skills

* Availability to travel if required

Personal Skills

* Dynamic, self-motivated, loyal, pro-active, goal-oriented, team-player

* Very good communication and presentation skills

* Good time and priority management

We offer:

* A responsible and independent role in professional and scientific environment and cooperation on exceptional projects

* Non-corporate company environment based on open communications, collaboration and friendly relationships

* Competitive salary package

* Company car


Informace o pozici

Společnost
AVENUE Consulting
Adresa
Praha
Požadované vzdělání: Vysokoškolské / univerzitní
Požadované jazyky: Čeština (Výborná), Angličtina (Pokročilá)
Zařazeno: Farmacie, Manažer klinických studií, Monitor klinických studií, Medical Advisor
Typ pracovního poměru
Typ pracovního poměru: Práce na plný úvazek
Délka pracovního poměru
Délka pracovního poměru: Na dobu neurčitou
Typ smluvního vztahu
Typ smluvního vztahu: pracovní smlouva
Zadavatel: Personální agentura