Senior Clinical Research Specialist - Chinese Speaking

at  Teckro Limited

ABOUT TECKRO

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
Could you be our newest Teckronaut?
Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.

QUALIFICATIONS REQUIRED:

• Degree in biological science, nursing, or other health-related discipline.
• Post graduate qualification in Clinical Research preferred.
• Proven competencies with Clinical Research methodologies and operational day to day activities.

TECKRO BENEFITS:

• 25 days holidays
• Pension
• 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
  We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
  By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro’s Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.

• Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team, to ensure timely delivery of high quality solutions
• Review study protocols/documents to identify areas of vulnerability and operational importance; customizing the platform to meet the requirements of individual studies
• Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client
• Review/analyze program/study-level risk registers/RACTs to assist in defining messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks.
• Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account
• Monitoring/analyzing of platform searches: identification of trends and unanticipated key variables; providing data to the development teams for product improvements.
• Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.
• Contribute to maintaining and improving in-house templates, SOPs and guides.
• Where required, assist in the Induction, training and upskilling of junior team members, mentoring and providing insight into Clinical Trial Operations.
• Undertake other duties in-line with your role and business requirements as required
• Regularly contribute ideas for innovation and product, quality and process improvements and additions