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Clinical Data Specialist
4 months ago
We are expanding We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.
Who are we?
- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence
- 20+ years of experience, ~500 people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe
- Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trial
- We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, cardiovascular and chronic diseases across various phases to improve the health of millions worldwide.
Why work with us?
- We are a global team making a difference in the world – our clinical trials improve the health of millions worldwide
- Competitive salary and benefits
- Flexible and agile working arrangements - onsite, hybrid or WFH (dependent on location)
- Strong and diverse Learning & Development opportunities including exposure to all aspects of clinical trials with an unparalleled network of Scientific Leaders to learn from
- A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities, and other fun events
Key Accountabilities:
- Work closely with the Data Management study leads in the assigned projects in allocated tasks
- Data listing review and checking the clinical database for inconsistent, missing, and incorrect data
- Generate queries to the sites to get the data clean, and ensure query resolution
- Review SAS listings and raise queries based on discrepancies
- Perform vendor file reconciliation (e.g. PK, ECG, Lab data, etc.)
- Generate reports and track data review progress
- Support data entry for all assigned projects
What are our expectations of candidates?
- M. Pharm/ Pharm. D/ B. Pharm fresher graduates
- Knowledge of Clinical Research/ Pharmacology/ diseases/ drugs/Contraindications/Clinical trial phases/Therapeutic Areas/Indications.
- Excellent time management and project management skills
- Excellent written and verbal communication skills
- Ability to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments
We are searching for individuals who are excited by the idea of regional and global projects and teams, don’t want to get lost in a large CRO and are ready to have their ideas heard
You will be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence.
How do I apply and what if I'm interested in a role in future or want to refer someone?
Apply via LinkedIn or send your CV, referral or confidential query to and our friendly HR team across the world will reach out as appropriate soon. Please provide your full contact details, the location you are applying for, whether you are interested in a current or future opportunity and we'll be in touch. We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.
How do I learn more about the roles and George Clinical?
Follow us on Linkedin to see our regular updates and how we celebrate our people and success across our business and projects You can also visit us at
We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.
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