Clinical Research Associate: Trial Monitoring & Compliance

Equilab International

Indonesia

On-site

IDR 100,440,000 - 167,400,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Equilab International in Indonesia is seeking a Clinical Research Associate to ensure GCP-compliant trial quality, manage study documentation, and support site activities from start-up to close-out.

You will prepare protocol and CRFs, assist Ethics Committee submissions, handle regulatory filings, perform site feasibility and monitoring, and act as the liaison between investigators and sponsors. Travel flexibility is required, and you should communicate clearly with diverse teams.

Qualifications

  • Bachelor Degree from Pharmacy or Science
  • At least 1 year experience as CRA, Regulatory/Registration in Pharmaceutical Companies, Clinical Research Industry or Hospital
  • Independent, detail-oriented and high compliance
  • Having good communication and negotiation skills
  • English proficiency is preferably
  • Open & flexible to travel

Responsibilities

  • Prepare clinical study documents (protocol, CRF, informed consent form, etc.)
  • Assist Principal Investigator for Ethics Committee submission
  • Responsible for Regulatory Affairs submission
  • Perform site feasibility, investigator selection, and site set up
  • Perform clinical trial monitoring, follow up and discussion with study site team
  • Responsible for maintaining trial documentation
  • Acting as a communication line between investigator and sponsor

Skills

Good communication
Project management
Negotiation skills
English proficiency
Willing to travel

Education

Bachelor degree (Pharmacy or Science)

Job description

Equilab International in Indonesia is seeking a Clinical Research Associate to ensure GCP-compliant trial quality, manage study documentation, and support site activities from start-up to close-out.

You will prepare protocol and CRFs, assist Ethics Committee submissions, handle regulatory filings, perform site feasibility and monitoring, and act as the liaison between investigators and sponsors. Travel flexibility is required, and you should communicate clearly with diverse teams.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Research Nurse: Study Coordination & Protocols
Clinical Research Nurse: Study Coordination & Protocols

Equilab International • Jakarta Selatan

On-site
IDR 90,000,000 - 130,000,000
Clinical Research Coordinator — Trials, Data & Patient Liaison
Clinical Research Coordinator — Trials, Data & Patient Liaison

Siloam Hospitals Group (Tbk) • Jakarta Utara

On-site
IDR 89,280,000 - 133,920,000
Clinical Research Associate
Clinical Research Associate

Equilab International • Indonesia

On-site
IDR 100,440,000 - 167,400,000
Site Study Physician — Clinical Trials Lead
Site Study Physician — Clinical Trials Lead

Oxford University Clinical Research Unit Vietnam (oucru) • Papua

On-site
IDR 223,200,000 - 390,600,000
Clinical Research Coordinator
Clinical Research Coordinator

Siloam Hospitals Group (Tbk) • Jakarta Utara

On-site
IDR 89,280,000 - 133,920,000
OUCRU ID – Site Study Physician – Keerom, Papua
OUCRU ID – Site Study Physician – Keerom, Papua

Oxford University Clinical Research Unit Vietnam (oucru) • Papua

On-site
IDR 223,200,000 - 390,600,000
Clinical Research Coordinator (Medan)
Clinical Research Coordinator (Medan)

Siloam Hospitals Group (Tbk) • Kota Medan ᯔᯩᯑᯉ᯲

On-site
IDR 120,000,000 - 180,000,000
QMS Associate II - Compliance & Training
QMS Associate II - Compliance & Training

Alcon Indonesia • Batam

On-site
IDR 133,920,000 - 200,880,000
Clinical Research Coordinator: Drive Protocols & Participant Care
Clinical Research Coordinator: Drive Protocols & Participant Care

Siloam Hospitals Group (Tbk) • Kota Medan ᯔᯩᯑᯉ᯲

On-site
IDR 120,000,000 - 180,000,000
QA Complaints & Regulatory Associate II
QA Complaints & Regulatory Associate II

Alcon Indonesia • Batam

On-site
IDR 120,000,000 - 180,000,000