Clinical Science Trainee
vor 14 Stunden
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences
That is why we in Switzerland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”
Severely disabled applicants will be given special consideration if they are equally qualified.
The focus of this entry position is to contribute to the scientific monitoring of clinical studies.
The incumbent is responsible for the compliance of the assigned tasks with department, company and regulatory standards and procedures.
**PRINCIPAL RESPONSIBILITIES**:
1. As requested and under the supervision of a SRS, contributes to the development of the clinical study protocol and of other clinical study documents, e.g. Informed Consent Form, Case Report Form, etc.
2. Participates in medical monitoring/ reporting including evaluation of adverse events.
3. Depending on the individual's experience, is the primary Clinical Science contact for external service provider(s) of a clinical study.
4. As requested and under the supervision of a SRS, contributes to and monitors daily activities of clinical studies which require scientific input, e.g. contribution to answers to trial-related Health Authorities' (HA) questions, answer to Ethic Committees /Institutional Review Boards questions, etc.
5. Ensures that all activities are in compliance with department, company and regulatory standards and procedures.
**Qualifications**:
**Required qualifications and experience**:
1. PhD, PharmD, DVM, MSc (or equivalent) degree in Biological Sciences required.
2. Knowledge of clinical development processes, clinical trial processes, and regulatory requirements/ ICH guidelines based on previous deliverables advantageous.
3. Excellent computer systems and software skills.
4. Excellent English.
**Competencies**
1. Good organizational skills, good written and verbal communication skills, able to work as part of a team and independently
2. Good independent time management skills advantageous
3. Ability to work well in a dynamic environment and be able to prioritize and respond to changing needs of the business.
4. Detail oriented.
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