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(senior) clinical project manager (m/f/d)

Leobendorf
Croma-Pharma
Director of Projects
€ 65.000 pro Jahr
Inserat online seit: 23 Juli
Beschreibung

CROMA-PHARMA is an internationally active pharmaceutical company with its headquarter in Leobendorf, Korneuburg district, in the north of Vienna. Many years of experience in the manufacturing of products based on hyaluronic acid and a unique level of expertise in the field of aesthetic medicine have made CROMA-PHARMA a globally renowned specialist in the dynamic and versatile business of anti-aging.

At Croma-Pharma, we are committed to developing and marketing innovative products that help our customers improve their well-being. Join us and grow with us.

Your future job

Planning, implementation, coordination and supervision of globally outsourced clinical trials

Project controlling (dates, cost, reporting, regular meetings, milestones)

Communication with the competent authorities and ethics committees

Preparation and Review of clinical submission documents for a regulatory audience, within a team environment, ensuring process, content, and submission

Organization and management of study relevant documents (from concept to archival)

Collaborating with and managing external partners (vendors, clinical research centers)

Implementation of audits from external vendors and study sites

Critical review and interpretation of clinical efficacy and safety data

Presentation of study results in the context of meetings

Active role in improvement of CROMA processes and implementation of agreed improvement steps

Creation and maintenance of SOPs, including development/improvement of appropriate workflows as relevant to clinical activities

Your Qualifications And Skills

Scientific degree, preferred PhD in life Sciences

Prior clinical project management experience (min. 5 years) or equivalent

Demonstrated experience in planning, monitoring, and conduct of clinical trials with medical devices and/or medicinal products/biologics

Knowledge of the processes of submission/implementation/completion of clinical trials with authorities

Familiarity with relevant laws, norms, standards, codes of practice and guidelines (e.g. ISO 14155, ICH-GCP)

Experience in writing/creating SOPs

Fluency in English and German (written and spoken)

We offer

Collective agreement for the chemical industry, 38 hours a week - the minimum gross salary according to the KV is EUR 59.781,96 for this position. The actual salary depends on the specific qualification and experience.

Flexible working hours and home office

Good public transport connections and free parking spaces

Croma restaurant with meal allowance and in-house fitness center

Pension and health care (company doctor and employee assistance programs)

Professional development

If you can imagine this position as the next step in your career, then apply online via our applicant portal so that we can treat your data confidentially and in compliance with the GDPR.

Our HR recruiting team will get in touch with you immediately.´

We are filling this position by ourselves - please no inquiries from headhunters and recruiters.

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