Medical Director/Study Physician - Austria - FSP

Parexel; Österreich; Remote; EUR 90.000 - 140.000; Vollzeit

Benefits dieser Stelle

Premium salary

Attractive benefits

Medical care plan: Health, Dental &amp

Zusammenfassung

Parexel FSP in Austria is looking for an experienced Study Physician to join a team supporting a key sponsor in the EMEA region. You will be medically responsible at the trial level throughout preparation, conduct and reporting phases, providing medical oversight from the Trial Design Outline to the Clinical Trial Report.

The role is a core part of the trial team, offering premium salary, attractive benefits and opportunities for growth across a global CRO environment.

Qualifikationen

• MD physician with clinical practice and trial support experience.
• Specialization in one or more medical fields is desirable.
• Experience in pharma/CRO environments is a plus.
• Understanding of ICH-GCP and clinical development processes.

Aufgaben

• Provide medical expertise and oversight throughout trial phases.
• Be medically responsible at the trial level from design to report.
• Support from Clinical Design Outline to Clinical Trial Report.
• Co-author Clinical Quality Monitoring plans and data reviews.
• Possess prior medical monitoring experience and IT/visualization skills.

Kenntnisse

MD Physician

Clinical practice 4+ years

Pulmonology

Immunology

Internal Medicine

Infectious Diseases

Family Medicine

Pediatrics

Rheumatology

Emergency Medicine

Ausbildung

Medical thesis preferred

Tools

Data visualization systems

IT systems

Jobbeschreibung

At Parexel FSP, you will be joining a team with a wide variety of experiences and knowledge.

We’re looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally.

We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.

Parexel is currently seeking an experienced Study Physician to join us in Austria, remotly. You be assigned to one of our key sponsors in the EMEA region.

Working as a Study Physician you will be medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial. During the clinical trial, you will be responsible to provide medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report.

This is a core role within the trial team.

Some Specifics About This Advertised Role

• Dedicated to one client.
• Ensure timely preparation of high medical quality clinical trial protocols, minimising protocol amendments.
• Contribute to trial risk-based quality management, by defining medically relevant data and related risks are integrated into the quality and risk management plan.
• Co-author Clinical Quality Monitoring plans.
• Performing ongoing reviews of medical data.

Here are a few requirements specific to this advertised role.

• Physician (MD) (ideally with medical thesis), trained in a clinical setting, and minimum of 4 years of active clinical practice experience; specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, and Emergency Medicine is highly desirable.
• Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions/ any other relevant medical function ideally in Clinical Development is desirable.
• Understanding of relevant regulations and guidance including ICH-GCP.
• Ideally previous experience as a medical monitor
• Ideally experienced with data visualization systems and IT systems.
• Clinical development/trials experience which would be an additional assets.

We will offer you

• Premium salary.
• Attractive benefits.
• Medical care plan: Health, Dental & Vision.
• Life Assurance.
• Pension plan
• Excellent work environment.
• Culture of teamwork and collaboration.
• People who motivate and face challenges together.
• Innovative technology.
• Excellent training.

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