Job Requirements
Skills
Job benefits
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Flexible work hours
Productivity curve is not something steady and consistent as it depends on each person's unique traits and preferences. At our company, as long as your team is in sync and your goal is hit, you can flexibly decide when you want to work.
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Remote work options
Thanks to technology, we no longer have to be physically present at the office to be productive. Joining our company allows you to work anywhere without place-constraint.
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Medical insurance
To ensure your health and wellbeing, you have various medical plans to choose from depending on your situation and unique needs. From partial up to full medical coverage, we got you covered.
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Team-building events
Our company simply cannot function well without teams of people working together. That said, we provide numerous team-building activities and events for you and your team to nurture meaningful relationships between every individual.
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Job description for Clinical Research Coordinator/Clinical Research Manager at Nalagenetics
- Minimum Education Qualification: Medical Doctor with Clinical Trial Experience or Master Degree in Life Sciences, Nursing, Public health, Pharmacy or related fields with minimum 2 years working experience as CRC/CRM
- 2 years’ experience in clinical research preferably.
- Experience in genetic testing or pharmacogenomic.
- Internal medicine, Neurology: in addition to the Psychiatry and breast cancer
- Research experience in breast cancer, psychiatry and cardiovascular would be an advantage.
- Experience in study design, ethical clearance approval, patient recruitment, data collection and analysis and study publications to ensure that studies are conducted in accordance with GCP and pre-specified protocols and can be completed in a timely manner
- Experience in data analysis and manuscript writing
- Good communications and interpersonal skills
- Good IT literacy and statistics skills
- Experience in administering basic clinical assessments
- Responsible and oversee clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines
- Oversee Project management, timeline, and daily operations
- Responsible and manage screening and recruitment of study subjects and coordination of subject visits.
- Perform data management, data analysis and manuscript writing
- Assist in all administrative requirements including submission process to IRB and/or regulatory authority
- Work closely with internal and external stakeholders to ensure all study-related activities are carried out efficiently
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