Manager, Clinical Affairs
2 weeks ago
To collaborate closely with Clinical Lead of Company / Medical Affairs department to set up the Medical Affairs of Company, develop strategies to enhance the effectiveness of its clinical quality program within the organisation and to identify and work on developing quality models, design and implementation of audits and risk management activities. To ensure accurate data collation and validation which includes clinical performance indicators, and timely submission to the Ministry of Health and various agencies. Additionally, to run Company's Quality Assurance (QA) and clinical services related committees. Duties and Responsibilities Primary Responsibilities and Duties (80%) Set up and run the following QA and clinical services committees in functions such as organising meetings, preparing relevant reports for meetings, recording minutes, and ensuring that follow-up actions are taken after the meetings. Not limited to: Clinical Committee which may comprise: Pharmacy, Therapeutics and Medication Safety Committee Credentialling and Privileging Committee Clinical Services, Medical Device and Procedures Committee Clinical Pathways Committee Clinical Ethics Committee Risk Management Committee which may comprise: Mortality, Morbidity and Peer Review Learning Committee Patient Safety Committee For clinical performance measurement: Monitor and collate data for Healthcare Performance Office QIP indicators - hospital wide clinical quality indicators Other indicators Collaborate closely with relevant data/ operations teams to ascertain the precision and validity of data, facilitating the timely submission of the performance indicators report to the Ministry of Health. Ensure that drafts for new or revised clinical forms, e.g., consent forms and clerking forms, are vetted by hospital lawyer if necessary and approved by GCMB/ Clinical Lead in a timely manner. Conduct JCI / ESS (or equivalent) activities. Conducting clinical audits for various clinical work processes, case notes audit / review, audits on problem cases and ad-hoc audits. Oversee the monitoring of mortality and morbidity reporting ensuring 100% reporting rate. Compile and analyse data and generate annual reports. Secondary Responsibilities and Duties (20%) Coordinate activities for Hospital Licensing Exercise and serve as liaison person for any queries on hospital licensing. (if required) Assist in preparing budget proposal (if required) Other Medical Affairs Activities Prepare presentations for HO / MO orientation (if required) Prepare papers for Medical Board, NUHS Board and MOH as and when required. Any other assigned duties Job Specification Bachelors degree with experience in a hospital setting. Experience in Quality Management/Assurance in an acute care hospital will be an added advantage. Computer skills in Words, Excel, Access and PowerPoint. Basic statistical skills. Keen interest in developing databases and reports relating to clinical QA. Strong interpersonal skills, be meticulous, self-initiated and independent. #J-18808-Ljbffr
-
Medical Affairs Manager
2 weeks ago
Singapur, Singapore Integrity Consulting Full timeMedical Affairs Manager / Clinical Affairs / Medical Devices MNC 1 day ago Be among the first 25 applicants We are looking for a candidate with accomplished experience in professional medical education and training development for your new company. It involves a mix of clinical leadership, KOL development, and evidence-based initiatives to enhance patient &...
-
Clinical Genomics
1 week ago
Singapur, Singapore Lucence Health Inc. Full timeClinical Genomics & Medical Affairs Specialist at Lucence About Lucence Lucence is advancing cancer care through precision oncology, delivering clinically actionable insights through next-generation sequencing (NGS) and liquid biopsy technology. Our work spans treatment selection, minimal residual disease (MRD), and multi-cancer early detection (MCED). About...
-
Clinical Genomics
2 weeks ago
Singapur, Singapore Lucence Full timeClinical Genomics & Medical Affairs Specialist Join to apply for the Clinical Genomics & Medical Affairs Specialist role at Lucence . About Lucence Lucence is advancing cancer care through precision oncology, delivering clinically actionable insights through next‑generation sequencing (NGS) and liquid biopsy technology. Our work spans treatment selection,...
-
Clinical Lead
5 days ago
Singapur, Singapore Emerald Clinical Full timeJoin to apply for the Clinical Lead role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We advance clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic...
-
Associate Director Regulatory Affairs
4 weeks ago
Singapur, Singapore Barrington James Full timeAn innovative and purpose-driven biotechnology, biologics company is seeking a Regulatory Affairs Associate Director to join its growing team. This role will be instrumental in shaping and executing global regulatory strategies, supporting clinical development across oncology and autoimmune programs. As a senior individual contributor, the Regulatory Affairs...
-
Director, Regulatory Affairs
2 weeks ago
Singapur, Singapore Ethos BeathChapman Full timeJoin to apply for the Director, Regulatory Affairs (APAC) role at Ethos BeathChapman 3 days ago Be among the first 25 applicants Global Contract Research Organisation (CRO) Location: Singapore (Flexible) We are an expanding global Contract Research Organisation (CRO) dedicated to advancing clinical research and improving patient outcomes worldwide. As part...
-
Clinical Project Manager
4 weeks ago
Singapur, Singapore CTI Clinical Trial and Consulting Services Full timeOverview Clinical Project Manager role at CTI Clinical Trial and Consulting Services. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the...
-
Director Regulatory Affairs
2 weeks ago
Singapur, Singapore Planet Pharma Full timeDirector of Regulatory Affairs We’re partnering with a leading global clinical research organization (CRO) seeking an experienced Director of Regulatory Affairs to lead regional regulatory strategy and execution across APAC. This position offers the opportunity to represent the company’s regulatory strategy meetings, and Health Authority interactions –...
-
Director, Regulatory Affairs
2 weeks ago
Singapur, Singapore BEATHCHAPMAN (PTE. LTD.) Full timeGlobal Contract Research Organisation (CRO) Location: Singapore (Flexible) We are an expanding global Contract Research Organisation (CRO) dedicated to advancing clinical research and improving patient outcomes worldwide. As part of our continued growth across the Asia‑Pacific region, we are seeking an experienced and visionary Director, Regulatory Affairs...
-
Scientific Affairs Mgr
1 week ago
Singapur, Singapore Bio-Rad Laboratories Full timeAs a Scientific Affairs Manager within Bio-Rad’s Clinical Diagnostics Division, the candidate supports the execution of global scientific strategies to drive clinical adoption of Bio-Rad’s technologies. This role bridges science and communication—transforming complex research into impactful materials and collaborations that enhance Bio-Rad’s...