Clinical Scientist - Early Development (m/f/d)

REFERENCE NUMBER:

497560/1

MY DUTIES:

-Your activities will include the development and writing of study documentation including protocols, informed consent forms, clinical study reports, as well as clinical science input for study-specific operational and regulatory documents
- You will be responsible for ongoing monitoring of clinical activities and study conduct, coordination of data collection, data review, analysis, and interpretation as well as preparation and presentation of results for informed decision-making. You will be the main point of contact for data management regarding periodic clinical data review and data cleaning
- You will participate in study management, as clinical science representative, to ensure trial deliverables are met according to timelines, budget, quality standards and operational procedures, within a global multidisciplinary cross-functional Study Management Team (SMT)
- You will provide training and science input to operation colleagues and study site staff, as agreed with clinical operations 
- You will monitor study progress on a regular basis to identify any problems or issues that could affect the results or completion of the study; you will investigate and employ problem-solving strategies
- You should bring a positive, energetic, responsible, creative, curious and solution-seeking mindset and proactively contribute to interdisciplinary clinical project teams with integrity, passion and courage

MY QUALIFICATIONS:

- Doctoral degree in a relevant scientific field (e.g. Neuroscience, Pharmacology, Psychology)
- Profound clinical science, in drug development and clinical trials methodology and execution (Phase 0-2 preferable)
- Experience with the design and conduct of clinical research studies in pharma or biotech
- Experienced with clinical data review, analysis, interpretation and reporting
- Familiar with ICH-GCP regulation and regulatory guidance documents about clinical trials
- Able to acquire knowledge in different disease indications and therapeutic areas
- Able to collaborate and thrive in a matrix environment and interact with a variety of individuals outside (e.g. investigators) and inside the company (e.g. regulatory affairs, biostatistics, clinical pharmacology, project management)
- Strong analytical and quantitative skills
- Strong project-management skills and ability to prioritize task in a dynamic environment
- Excellent written and oral communication skills in English
- Strong communication skills and ability to interact in a cross-functional matrix and represent science in study management teams, projects team and across the whole organization

MY BENEFITS:

- You will work in an international environment

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

MY CONTACT AT HAYS:

My contact person
Emina Mustafic

Reference number
497560/1

Contact
E-Mail: [email protected]
Phone: +41-(0)61-2250518