Clinical Scientist

7 days ago

Athens, Attica, Greece Veeda Lifesciences Full time €30,000 - €60,000 per year

Veeda Lifesciences is seeking a Clinical Scientist based in Athens (Greece) for its growing international hematology/oncology Clinical Trials program.

The Clinical Scientist is responsible for providing medical input within the organization as well

as to external partners and performing medical review tasks within the context of clinical trials.

Furthermore, the Clinical Scientist is responsible for undertaking scientific/medical writing tasks

within the organization.

This is a full-time job.

Required Qualifications:

  • MD or PhD in Health Sciences.

-BSc/MSc degree combined with exceptional work/research experience is also in line with the organization's requirements for this role.

-1 year of experience in a CRO or in the pharma industry in a relevant role (Clinical, Medical Information or Medical Affairs)

-Exceptional written and oral use of English

−Excellent communication skills

−Excellent business acumen

−Initiative taking and team working attitude

−Excellent Organizational skills

−Innovative thinking

−Excellent IT skills

−Deep understanding of the Clinical Development industry

Main responsibilities:

− Is responsible for the development of:

  • All study related documents that fall under the Clinical Science Department scope (e.g., Study Protocols, ICFs - in collaboration with other departments e.g., Clinical Operations, Regulatory, as required -, Pharmacy Manuals, Medical Review Plans, etc.)
  • Scientific presentations and manuscripts
  • Medical training material (i.e. therapeutic area and study protocol training material)

− Delivers internal and external study protocol and therapeutic area training courses

− Provides medical input within the Company on key therapeutic areas of the assigned clinical trials/projects

− Provides guidance to the Project Management and Clinical Operations departments on the medical and scientific aspects of the assigned clinical trials/projects

−Responds to medical queries from all involved parties in assigned clinical trials (e.g., CRAs, Project Managers, Clinical Operations Managers, Investigators) and collaborates with all concerned staff in maintaining an up-to-date study-specific Q&A log

−Is available 24/7 to respond to urgent medical/protocol related issues derived from an Investigational Site, as applicable

− Performs periodic medical review of the data from clinical trials according to the study specific

Medical Review Plan requirements (e.g., review of eligibility, review of efficacy and safety data listings)

−Collaborates with and provides medical input to the Data Management staff to ensure the successful development of the study-specific eCRF

−Attends Investigator Meetings and Conferences, as applicable

Why join us:

Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.

In depth training and support will be provided.

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