1-Month Career Trial

Position DetailsFull Time Position44 hours work per week, shift work & no fixed rest day. (6 days off in a month)Career Trial ObjectivesProvide potential candidates with hands-on experience in the F&B industry, allowing them to explore the service crew career paths, showcase their skills, and determine mutual fit before committing to a full-time position...

Clinical Trial Assistant (1-Year Contract) - FMCG MNC #HHL Singapore | Posted: Dec 06, 2024 Location: Boonlay (West)Duration: 1-year contract starting January 2025Salary: Up to $4650 + 1 month completion bonusWorking Hours: 5 days, office hoursKey Responsibilities:Manage and maintain electronic Trial Master Files (e TMFs).Oversee CROs, develop e TMF...

Clinical Trial Assistant (1-Year Contract) - FMCG MNC #HHL Singapore | Posted: Dec 06, 2024Location: Boonlay (West)Duration: 1-year contract starting January 2025Salary: Up to $4650 + 1 month completion bonus Working Hours: 5 days, office hours Key Responsibilities: Manage and maintain electronic Trial Master Files (eTMFs). Oversee CROs, develop eTMF...

Roles & Responsibilities1 Year Contract Clinical Trial AssistantWestBudget : up to $4650 with completion bonus 1 month. Jobscope:•Supports high-quality electronic Trial Master Files (eTMFs). Performs set-up, maintenance (filing and approving documents) and archiving of eTMFs. •Provides CRO oversight by developing eTMF guidelines, establishing review...

Location: Boonlay (West)Duration: 1-year contract starting January 2025Salary: Up to $4650 + 1 month completion bonusWorking Hours: 5 days, office hoursKey Responsibilities:Manage and maintain electronic Trial Master Files (eTMFs).Oversee CROs, develop eTMF guidelines, and ensure complete filing.Document clinical studies in compliance with GCP and...

Job Description:We are seeking a highly skilled and experienced Senior Clinical Trials Specialist to join our team at the National Cancer Centre of Singapore PTE LTD. As a key member of our clinical trials operations team, you will play a critical role in ensuring the successful conduct of clinical trials.About the Role:You will be responsible for...

At Recruit Express Pte Ltd, we are seeking a skilled Clinical Trial Assistant to join our team. This role is responsible for supporting the maintenance of clinical studies and ensuring compliance with Good Clinical Practices (GCP) and relevant Standard Operating Procedures (SOPs).Key Responsibilities:Supports the setup, maintenance, and archiving of...

Medpace is a leading full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. With over 5,000 employees across 40+ countries, we provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are committed to...

Job Description Summary Internal Role Title: Clinical Trial Associate Location: Singapore #LI-Hybrid About the Role: The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in assigned studies during set-up and whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements....

About ICON CLINICAL RESEARCH (PTE) LIMITEDAt ICON, we're a global leader in clinical research with over 40,000 talented individuals working together across 40 countries. We empower our people to excel in their careers and contribute to making a meaningful difference in the lives of patients.Job OverviewWe're seeking an experienced Clinical Trials Specialist...

Summary The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in assigned studies during set-up and whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements. Key Responsibilities: Supports document collection, preparation, and adaptation for submission to IRB/EC and...

Location: Boonlay (West)Duration: 1-yearcontract starting January 2025Salary: Up to $4650 + 1month completion bonusWorking Hours: 5 days, officehoursKey Responsibilities:Manage and maintain electronic Trial Master Files(eTMFs).Oversee CROs, develop eTMF guidelines, andensure complete filing.Document clinical studies incompliance with GCP and SOPs.Support...

About TUMCREATE TUMCREATE is a multidisciplinary research platform of the Technical University of Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies. Please visit for more information about...

Roles & ResponsibilitiesAbout TUMCREATETUMCREATE is a multidisciplinary research platform of the Technical University of Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.Please visit...

Roles & ResponsibilitiesAbout TUMCREATETUMCREATE is a multidisciplinary research platform of the Technical University of Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.Please visit...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...

Roles & ResponsibilitiesDuration 1 year (Start end Feb 2025)Salary : up to 4500Location: Boon LayJobscope:•Supports high-quality electronic Trial Master Files (eTMFs). Performs set-up, maintenance (filing and approving documents) and archiving of eTMFs. •Provides CRO oversight by developing eTMF guidelines, establishing review processes, and ensure the...

Roles & ResponsibilitiesDuration 1 year (Start Jan 2025)Salary : up to 4500Location: Boon LayJobscope:• Supports high-quality electronic Trial Master Files (eTMFs). Performs set-up, maintenance (filing and approving documents) and archiving of eTMFs.• Provides CRO oversight by developing eTMF guidelines, establishing review processes, and ensure the...

Roles & ResponsibilitiesDuration 1 year (Start Jan 2025)Salary : up to 4500Location: Boon LayJobscope:• Supports high-quality electronic Trial Master Files (eTMFs). Performs set-up, maintenance (filing and approving documents) and archiving of eTMFs.• Provides CRO oversight by developing eTMF guidelines, establishing review processes, and ensure the...