Coordinator jobs in Malaysia
Senior Clinical Research Associate I (SCRA1), FSP model
Fortrea
Utility Technician (Process)
GS Paperboard & Packaging Sdn Bhd
Contract & Admin Coordinator (Fresh Graduates Welcome)
Innovans Palm Industries Sdn. Bhd.
Bilingual Customer Service & Sales Support Specialist
PROMAID SERVICES & SUPPLIES Sdn Bhd
Immigration & Foreign Worker Admin Coordinator
Oka Concrete Industries
Discover more opportunities than anywhere else. Find more jobs nowSenior 3PL & Inventory Optimization Lead
Grace And Glow
Cashier Supervisor & Operations Coordinator
Trendcell
Connect with headhunters to apply for similar jobsAdmin & Customer Service Coordinator
Three D Kitchen Cabinet
Safety & Health Officer (Facility Management)
Vfive Group
Clinic Nurse & Care Coordinator
KLINIK SERI KINRARA SDN. BHD.
Dental Admin & Patient Care Coordinator
BP Healthcare Group
Customer Service & Logistics Coordinator
Accurativ (M) Sdn Bhd
Sales Operations & Customer Support Coordinator
Rapha Medical
Project Admin & Documentation Coordinator
Jobstreet Malaysia
Indoor Sales & Sourcing Coordinator
Fuji Koki Resources (M) Sdn Bhd
Indoor Sales Coordinator
Fuji Koki Resources (M) Sdn Bhd
ENT Clinic Assistant & Patient Flow Coordinator (FT/PT)
Sunway Klinik ENT
Senior Clinical Research Associate I
Job summary
A leading clinical research company is seeking a Senior Clinical Research Associate I to oversee site monitoring and management of clinical studies. You will be responsible for ensuring compliance with project plans and regulatory guidelines, contributing to the drug development process. Ideal candidates will have a degree in life sciences or relevant experience and be fluent in English. This role requires strong monitoring and management skills, along with the ability to work independently.
Qualifications
- Minimum 3 years of relevant clinical research experience.
- Thorough knowledge of regulatory requirements.
- Fluent in English and local language.
Responsibilities
- Monitor and manage clinical study sites.
- Ensure compliance with project plans and SOPs.
- Conduct pre-study and initiation visits.
Skills
Education
The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of scope, as assigned. Assume line management responsibilities, as assigned. Act in the project role of a Local Project Coordinator or Lead CRA as assigned.
Summary of Responsibilities:
Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
Responsible for all aspects of site management as prescribed in the project plans.
Qualifications (Minimum Required):
University or college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
In lieu of the above education requirement, candidates with a minimum of 3 years relevant clinical research experience in pharmaceutical or CRO industries will be considered.
Thorough knowledge of regulatory requirements including a basic understanding of regulatory requirements in other countries.
Thorough understanding of the drug development process.
Fluent in local office language and in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
Typically Three (3) years of clinical onsite monitoring experience.
Have a full understanding of Serious Adverse Event (SAE) reporting, process production on reports, narratives and follow up of SAEs.
Advanced site monitoring skills.
Advanced study site management skills.
Advanced registry administration skills.
Ability to work with minimal supervision.
Valid Driver's License.
Physical Demands/Work Environment:
Learn more about our EEO & Accommodations request here.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.