Site relationship management role ensuring sustainable trial start - up for assigned sites in clinical drug development at Novartis. Collaborating with global teams and ensuring adherence to clinical operations standards and timelines.
About the role
- Clinical Research Specialist responsible for analyzing complex biomedical information and mentoring junior staff in clinical operations for Teckro. Ensuring timely delivery of clinical trial solutions while working in a hybrid model.
Responsibilities
- Analyse, understand, and process complex scientific/medical/pharmaceutical information
- Working closely with the Senior CRS, execute the layout and structure of clinical information required to utilize our products efficiently and effectively
- Involved in the assessment of client documents prior to project development to determine project timelines
- Work with internal project teams and study team timelines to ensure timely delivery of high-quality solutions
- Assisting with the updating of clinical operations process guides
- Responsible for quality checking projects as part of risk assessment
- Contribute to process and product updates, working closely with other Teckro teams such as software and the product team.
- Communicate effectively within the team and also across other Teckro teams regularly
- Responsible for the training, mentoring and development of CRS level 1, including the preparation and development of training materials and tools
- Undertake other duties in-line with your role and business requirements as required
Requirements
- Degree in biological science, nursing, or other health-related field
- Some clinical trials experience, preferably in the clinical operations setting of clinical trials, understanding the day to day needs, risks and blockers of clinical trial teams.
- A good understanding of ICH / GCP and essential clinical trial documents.
- Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the clinical trials area in Teckro.
- Excellent computer skills
- Excellent communication skills.
Benefits
- 25 days holidays, entitlement increases with length of service
- Pension, available immediately upon joining Teckro
- Healthcare
- Life Insurance
- Share Options
- 50% Maternity leave pay after capped length of service
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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