Areas: Ampang, KL
Responsibilities
- Review patient medical records and extract relevant clinical and treatment data.
- Accurately enter and verify study data in the electronic Case Report Form (eCRF).
- Support data cleaning, discrepancy resolution, and database completion activities.
- Liaise with the Principal Investigator and study team to ensure timely study progress.
- Maintain confidentiality and accurate study documentation.
- Ensure compliance with study protocol, GCP, ethical standards, and applicable regulations.
- Participate in study-related meetings and training as required.
Requirements
- Master/Degree in a relevant healthcare or life sciences discipline.
- 1 year experience in clinical research, observational studies, registry studies, or data entry activities.
- Fresh graduate is encourage to apply
- Applicant with knowledge of hematology, oncology, CML, and/or MPN disease areas is added advantage .
- Has knowledge of clinical trials and GCP certification.
- Meticulous, detail-oriented, multitask, adaptable, and well-organized.
- Able to work independently to meet milestones and project deliverables.
- Has excellent communication and interpersonal skills.
For those who have what it takes, please apply online or send in your profile to:
Consultant: Janice Lim
Tel: ************* 8440
For more job opportunities, please visit:
For more job opportunities, please visit *************
OUR SERVICE FOR JOB SEEKER IS FREE!
Job Type: Contract
Pay: RM2,400.00 - RM3,000.00 per month