Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • Zuchwil

Description

Caring for the world… one person at a time” … inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo
 
DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, we created one organization that will be agile and better equipped in today’s evolving health care environment. Our broad array of inspired, innovative and high-quality offerings help advance the health and wellbeing of people around the world.
 
For our EMEA headquarters in Zuchwil, Solothurn we are looking for an experienced

Staff Clinical Research Scientist

your responsibilities:

Support non-regulated (Investigator Initiated, Registries, or company sponsored post-market studies) and regulated studies (IDE, HDE, Post-Approval, 522). 
Assist with high complexity studies and may support components
Participate in product development Project Core Team (PCT) activities and provide input and complete clinical tasks
Support front end activities related to clinical feasibility including literature reviews
Support Clinical Evaluation Reports for new products
Support development of evidence generation and publication strategies with input from cross functional teams
Support the progress of assigned Investigator Initiated Studies, including interacting with the primary Investigator and site staff, verify milestones, track budgets, and generate evidence according to agreements
Develop collaborative relationships with other functional areas within the Office of Science and Technology and the Operating Company
Develop strong collaborative relationships with Study Core Team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders
Support maintainance of registration on www.clinicaltrials.gov from study initiation through posting of results
Support collaboration with investigators and internal stakeholders to support publication strategy execution
May support the review of clinical information required for periodic safety and post-market surveillance reviews in collaboration with Medical Affairs
Apply high standards of critical thinking, analysis, collaboration, and communication for the advancement of clinical programs
Develop a strong understanding of the Operating Company product portfolio and pipeline, and business needs
Keep management informed of key developments and issues that impact clinical strategy and portfolio management
Ensure the completion of required templates and documents, and maintenance of records
May be involved in other tasks to support clinical research activities or Operating Company as needed
Consistently strive to improve the performance, reputation, and image of the clinical organization
Ensure efficient use of resources to provide high quality deliverables
Know, understand, incorporate, and comply with all applicable laws and regulations relating to DePuy Synthes business activities, and Policies and Procedures of the Health Care Compliance Program and Code of Conduct
Provide quality feedback to the Directors and Managers of each resource assigned to clinical studies regarding employee performance within the context of the clinical studies

Qualifications
BS/BA or equivalent, preferably in Life Sciences, Biomedical Engineering, or related field required.
Advanced medical science or medical degree is desirable
Understanding of Good Clinical Practices
Application of scientific research principles
Understanding and application of regulations and standards applied to medical device clinical research
Desirable minimum durations of relevant experience: BSc with 7+ years; Master’s with 5+ years; PhD/MD/PharmD with 3+ years
Previous clinical research or related technical experience required; orthopaedic

About the company

If you’re thinking about taking your career to a place where you can be seen for the talent you bring to your work, where you’ll have a chance to be the driver of your own career, and where others share your passion for caring and success, then we invite you to explore Johnson & Johnson. BE VITAL in your career and make a unique mark. Join the approximately 129,000 men and women who work within our companies and touch the lives of more than a billion people around the world every day.

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