Posição: Associate

Tipo de empregos: Full-time

Loading ...

Conteúdo do emprego

Hobson Prior are currently looking for a Clinical Scientist to join a fantastic organisation on a contract basis located in Basel. Our client is focused on creating medications for patients. For more information, please get in touch now!

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities
  • 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.
  • The ideal candidate will be responsible for bringing a positive, energetic, creative and solution-seeking mindset and to proactively contribute to interdisciplinary clinical project teams. The values of integrity, passion, courage, scientific curiosity, humility and responsibility, are important for success in the role.
  • You will contribute to experimental medicine studies and/or projects in collaboration with internal or external Partners.
  • The activities you are responsible for 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.
  • Responsible for ongoing monitoring of clinical activities and study conduct, coordination of data collection, data cleaning and review, analysis, and interpretation as well as preparation and presentation of results for informed decision-making.
  • 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 will collaborate with internal experts, leading academics, and external industry-based authorities and providers regarding experimental medicine and translational medicine studies
  • You will stay at the forefront of scientific and technical excellence by collaborating with the scientific community, contributing to presenting and publishing high-quality scientific abstracts, posters, articles and participating in key conferences
  • You will contribute to experimental medicine studies and/or projects in collaboration with internal or external Partners.
Key Skills
  • Excellent analytical and quantitative skills.
  • Excellent written and oral communication skills in English.
  • Familiar with ICH-GCP regulation and regulatory guidance documents about clinical trials.
  • The ideal candidate will have good project-management skills and ability to prioritize tasks in a dynamic environment.
  • 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.
Requirements
  • Doctoral degree in a relevant scientific field (e.g. Neuroscience, Pharmacology, Psychology // PhD, Pharma D or MD).
  • A minimum of 1-2 years in Clinical Science (experience in conducting on ongoing trials, collaboration with the operations team, vendor, site management).
  • Industry experience (Pharma / Medical - not Medical Devices).
  • You will require experience in drug development and clinical trials methodology and execution (Phase 0-2 preferable).
  • Experienced with clinical data review, analysis, interpretation and reporting.
  • Experience in Neuroscience as a Clinical Scientist (especially in movement disorders and/or neurodegeneration).
  • Track-record of impactful scientific research.
  • Ability 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, partners, KOLs) and inside the company (e.g. regulatory affairs, biostatistics, clinical pharmacology, project management).
Apply Now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
Loading ...
Loading ...

Data limite: 13-05-2024

Clique para aplicar para o candidato livre

Aplicar

Loading ...
Loading ...

EMPREGOS SEMELHANTES

Loading ...
Loading ...