1,100+ Plc Jobs - October 2026 - Urgent Hiring

Showing 1,111 jobs results for "plc"
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Prudential Plc

Outram

Posted
4 days ago

Clementi

Posted
4 days ago

Clementi

Posted
4 days ago

Outram

Posted
4 days ago

Clementi

Posted
4 days ago

Clementi

Posted
4 days ago

KL City

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct. ...
Posted
4 days ago

KL City

  • Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
  • Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.
  • Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle. ...
Posted
4 days ago

ICON Plc

KL City

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct. ...
Posted
4 days ago

KL City

  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
  • Support the preparation of study-related materials, such as informed consent forms and case report forms. ...
Posted
4 days ago

ICON Plc

KL City

  • Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
  • Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively. ...
Posted
4 days ago

KL City

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct. ...
Posted
4 days ago

KL City

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. ...
Posted
4 days ago

KL City

  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders. ...
Posted
4 days ago

KL City

  • Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
  • Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
  • Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study. ...
Posted
4 days ago

Singapore

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. ...
Posted
11 days ago

KL City

  • Design, develop, and deploy machine learning models for fraud and AML detection, supporting both batch and real-time transaction scoring scenarios.
  • Build and maintain MLOps pipelines covering model training, validation, deployment, monitoring, and retraining workflows using modern tooling (e.g. MLflow, Tecton, or equivalent feature stores).
  • Collaborate with data engineers to design feature engineering pipelines and maintain the Predator feature dictionary and sync mechanisms. ...
Posted
14 days ago

ICON Plc

KL City

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct. ...
Posted
15 days ago

KL City

  • Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
  • Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.
  • Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle. ...
Posted
15 days ago

KL City

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct. ...
Posted
15 days ago

ICON Plc

KL City

  • Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
  • Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively. ...
Posted
15 days ago

Clementi

Posted
15 days ago

Clementi

Posted
16 days ago

Clementi

Posted
17 days ago

Outram

Posted
17 days ago

Singapore

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. ...
Posted
17 days ago

Singapore

  • Well Established Company
  • Basic $3500 - $4500 + Allowance + Variable Bonus
  • Excellent Welfare and Benefits + Career progression ...
Posted
24 days ago

George Town

  • Request campaign inventory and collaborate with internal teams to establish program parameters and develop client recommendations
  • Price products for contract components across multiple formats, including CPQ forms and agency templates (Excel)
  • Execute pre-sale data requests for all Informa TechTarget initiatives ...
Posted
3 days ago

George Town

  • Request campaign inventory and collaborate with internal teams to establish program parameters and develop client recommendations
  • Price products for contract components across multiple formats, including CPQ forms and agency templates (Excel)
  • Execute pre-sale data requests for all Informa TechTarget initiatives ...
Posted
3 days ago

George Town

  • Request campaign inventory and collaborate with internal teams to establish program parameters and develop client recommendations
  • Price products for contract components across multiple formats, including CPQ forms and agency templates (Excel)
  • Execute pre-sale data requests for all Informa TechTarget initiatives ...
Posted
3 days ago