16 Clinical Development jobs in Singapore

Position Overview

We are seeking an accomplished Clinical Development Director/Senior Director to join our global R&D team. Based in Singapore and reporting directly to the Group R&D Head, this individual will play a pivotal role in shaping and executing medical strategies for drug candidates in preparation for global market launch. The ideal candidate will bring extensive expertise in vaccine-related projects, coupled with strong regulatory knowledge and cross-border collaboration experience.

Key Responsibilities

Lead the design and implementation of clinical development strategies, ensuring alignment with global regulatory requirements and commercial objectives.

Drive clinical research programs for vaccine and therapeutic projects from early development through global launch readiness.

Provide scientific and medical leadership to cross-functional teams, including regulatory affairs, clinical operations, pharmacovigilance, and medical affairs.

Act as a key liaison with global regulatory agencies (e.g., US FDA, EMA, HSA/Health Sciences Authority Singapore) to facilitate successful clinical trial applications, approvals, and submissions.

Evaluate and integrate new clinical insights, emerging trends, and competitive intelligence into the company's clinical development roadmap.

Build and maintain strong collaborations with external KOLs, research institutions, and industry stakeholders to support global clinical programs.

Mentor and guide junior clinical development team members to strengthen organizational capabilities.

Qualifications & Requirements

MD or PhD in Medicine, Pharmacology, Immunology, or related life sciences discipline.

Minimum 10 years of progressive experience in clinical development within the pharmaceutical or biotechnology industry, with a strong track record in vaccine-related programs.

Proven experience in developing and executing global clinical development strategies, ideally from Phase I through registration.

Prior direct interactions and established networks with regulatory authorities such as the US FDA, European EMA, and Singapore's HSA are highly desirable.

Demonstrated ability to lead cross-functional and multicultural teams across global locations.

Strong analytical, strategic, and problem-solving skills with an ability to make sound clinical and business decisions.

Excellent communication and presentation skills; ability to influence senior stakeholders and external partners.

Fluency in both English and Chinese is required to support cross-border collaboration within the group and with international regulatory agencies.

You will be part of the operational team in Clinical Trials & Research Unit (CTRU). You will work alongside members of the project team to provide project management service for projects that fulfil eligibility criteria under oversight of the Project Manager.

Responsibilities:

• Able to lead or facilitate project discussions independently, effectively and efficiently
• Ensure smooth and effective conduct of research projects according to applicable regulations by informed study teams

• To assist Principal Investigators in project organization which includes the following:

• Budget estimate and planning

• Grant(s) application (if applicable)
• Submission to ethics and regulatory bodies, and tracking the approval status
• Sourcing for external vendors/suppliers and assisting in negotiation of acceptable costs
• To manage, guide, supervise and review the performance evaluation of the project team members and review the quality of the work completed by the project team on a regular basis
• To assist in the drafting of relevant project progress reports including the analysis, interpretation and reporting process of findings and results as well as to assist in the preparation of manuscripts, reports and presentation materials (if applicable)
• Assist in the review and implementation of department SOPs and work instructions
• To take on projects as assigned from time to time

Requirements:

• Degree in Life Sciences/ Pharmaceutical Science/ Clinical Trials Management
• At least 4 years relevant experience in clinical project management. Those with advance proficiency in Project Management and expert knowledge of trial procedures, institutional, CIRB & regulatory authority requirements for managing clinical trial would be at an advantage
• Team Player and ability to multi-task, with good time management
• Self-motivated and ability to work in a fast-paced environment
• Good interpersonal relationship skills

Job Summary

We are seeking a highly organized and detail-focused individual to fill the Clinical Trial Admin Assistant role.

• Schedule study-related appointments for research subjects, ensuring timely and efficient completion of tasks.
• Complete data collection forms accurately and promptly, maintaining high levels of quality control.
• Conduct surveys or questionnaires as required, gathering valuable insights to inform study outcomes.
• Manage study-related equipment, guaranteeing optimal performance and minimizing downtime.
• Handle queries from research subjects in a professional and courteous manner, providing clear guidance and support.

• Able to work independently with minimal supervision, demonstrating self-motivation and discipline.
• Able to adapt quickly in a fast-paced environment, prioritizing tasks effectively and managing multiple responsibilities.

Job Opportunity: Clinical Trial Assistant

• Schedule appointments and manage study-related tasks for research subjects.
• Conduct surveys and gather data through questionnaires.
• Manage equipment and supplies necessary for the study.
• Handle queries from research participants in a professional manner.

• Able to work independently with minimal supervision.
• Adapt quickly to changing environments and priorities.

Interested applicants may send their resume in MS Word format to Cameron in the Outsourcing Team at Recruit Express Pte Ltd, EA License No. 99C4599.

Clinical Research Nurse

The successful candidate will be responsible for screening study participants according to regulatory guidelines and ethical standards.

• Conduct informed consent discussions and ensure participants understand the study's requirements.
• Monitor patient progress and collect data during clinical trials, ensuring accurate documentation.
• Administer study-related interventions as per protocol, including medications and treatments.
• Conduct assessments and follow-ups with participants, addressing any concerns and providing education.

Key Responsibilities Include:

• Screening and enrollment of patients in accordance with protocol.
• Collection of data from patients during their participation in studies.
• Monitoring of patients' responses to treatment and collection of relevant data.
• Assessment of patient safety and reporting of any adverse events or reactions.

• Diploma/Degree in Nursing
• Valid SNB & BCLS required
• Able to perform IV Cannulation and Phlebotomy

This role offers a unique opportunity to work on cutting-edge research projects while developing your clinical skills and knowledge.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
As a Biotechnologist at Lonza Mammalian business, you’ll be part of our globally recognized network, driving the production of mammalian cell culture and treatments.
Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation and make a difference from day one. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Daily company bus from the MRT location near your home to and from the Tuas site.
Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
The full list of our global benefits can be also found on
What you’ll do:
Perform GMP manufacturing operations, equipment handling, and troubleshooting.
Maintain facility and lab standards through sanitization and 6S housekeeping.
Apply aseptic techniques for material and cell culture handling.
Operate bioreactors, monitoring pH/DO, CO2/O2, and cell performance.
Execute chromatography, ultrafiltration, and pH/conductivity adjustments.
Utilize process control systems (UNICORN, DeltaV) and documentation (SOPs, logbooks, BRs).
Handle single-use technologies and sample submissions via LIMS.
Prepare customer-specific solutions and set up equipment for operations (CIPs, buffer transfer).
Plan and execute CIPs (downstream), ensuring correct pathways and configurations.
What we’re looking for
Degree or diploma in a related Science/Engineering field.
Knowledge of Biopharmaceutical processing is an added asset.
Relevant work experience in a similar manufacturing industry or cleanroom environment preferred.
Knowledge of cGMP applications.
Positive team oriented demeanor.
Strong communication and interpersonal skills.
Willing to perform a rotating 12-hour shift pattern.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
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Main Duties
Assist to review clinical trial contracts and work closely with the SingHealth Legal Department to negotiate agreement terms with commercial sponsors, CROs, academic institutions or international trial groups.
Assist in checking hard copy contract documents and obtaining signatures from the NCCS’s signatories.
Keep track of agreement timelines and chase for replies if a party has not replied for the past two weeks.
Supervise and provide advice to the executives of the Feasibility Team in NDA negotiation and to act as back-up for such review and negotiation during manpower shortage.
Assist in approving online payments in APIMS, training applications in PeopleConnexion (SuccessFactors)and any other online applications assigned.
Help to oversee financial and insurance reporting to CTCC as well as annual NMRC reporting.
Assist in submission and updating of the clinicaltrials.gov, check and approve archiving costs and payment to archiving company and MRO.
File and maintain executed contracts and ensure these are stored securely to maintain confidentiality and prevent loss or damage.
Perform any other duties assigned by the supervisors or the Clinical Trials Office higher management staff
Main Requirements
A recognised degree, with at least 6 to 8 years of relevant experience in negotiating clinical trial contacts or research study contracts as well as experience in staff supervision.
Preference for individuals with good knowledge of clinical trial conduct procedures.
Well versed in relevant laws and regulations applicable to trial conduct including HBRA, Health Products and Medicines Act, Health Product (Clinical Trial) Regulation, PDPA and ICH GCP.
Strong communication and writing skills, good command of language, good people skills and strong ability to be a good team player.
Strong leadership and management skills.
Meticulous, sharp and driven
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You will be part of the operational team in Clinical Trials & Research Unit (CTRU). You will work alongside members of the project team to provide project management service for projects that fulfil eligibility criteria under oversight of the Project Manager.

Responsibilities:

• Able to lead or facilitate project discussions independently, effectively and efficiently
• Ensure smooth and effective conduct of research projects according to applicable regulations by informed study teams

• To assist Principal Investigators in project organization which includes the following:

• Budget estimate and planning

• Grant(s) application (if applicable)
• Submission to ethics and regulatory bodies, and tracking the approval status
• Sourcing for external vendors/suppliers and assisting in negotiation of acceptable costs
• To manage, guide, supervise and review the performance evaluation of the project team members and review the quality of the work completed by the project team on a regular basis
• To assist in the drafting of relevant project progress reports including the analysis, interpretation and reporting process of findings and results as well as to assist in the preparation of manuscripts, reports and presentation materials (if applicable)
• Assist in the review and implementation of department SOPs and work instructions
• To take on projects as assigned from time to time

Requirements:

• Degree in Life Sciences/ Pharmaceutical Science/ Clinical Trials Management
• At least 4 years relevant experience in clinical project management. Those with advance proficiency in Project Management and expert knowledge of trial procedures, institutional, CIRB & regulatory authority requirements for managing clinical trial would be at an advantage
• Team Player and ability to multi-task, with good time management
• Self-motivated and ability to work in a fast-paced environment
• Good interpersonal relationship skills

Only shortlisted candidates will be notified

Project Officer (Clinical Trials & Translational Research) page is loaded# Project Officer (Clinical Trials & Translational Research)locations:
NTU Main Campus, Singaporetime type:
Full timeposted on:
Posted Todayjob requisition id:
R **Join Our Team at the School of Biological Sciences, Nanyang Technological University, Singapore**The School of Biological Sciences (SBS), part of the College of Science, was established in 2002 with a mission to advance biological and biomedical sciences. At SBS, our research spans various areas, including infectious diseases, immunology, neurodegenerative diseases, telomere biology, and genome function. Over the years, SBS has attracted talented individuals from around the world and Singapore to join as scientific leaders and researchers.For more details, please view are looking for a Project Officer to join the Yang Lab at NTU ( The successful candidate will contribute to an interdisciplinary project evaluating the clinical efficacy and biological mechanisms of traditional, complementary, and integrative medicine (TCIM) interventions for symptom management in cancer populations.The role will focus on coordinating clinical trials and supporting laboratory operations, bridging patient-centered trial activities with bench-based biospecimen handling and multiomics investigations. Through this work, the candidate will be well-positioned to grow at the interface of clinical and laboratory science, while shaping a distinctive academic and professional trajectory.**Key Responsibilities:*** Coordinate randomized clinical trials, including ethics/IRB application and regulatory compliance* Manage trial logistics, patient recruitment, scheduling, and follow-up* Oversee collection, processing, and management of clinical data and biospecimens* Conduct data entry, curation, quality control, and preliminary analyses* Oversee laboratory operations, ensuring compliance with institutional and local safety regulations and good laboratory practices* Manage procurement of equipment, reagents, and consumables* Train and onboard new research staff and students* Liaise with clinical collaborators, institutional partners, and external stakeholders* Support project reporting and documentation for funding and administrative purposes**Job Requirements:*** Bachelor’s degree in life sciences, biomedical sciences, public health, social sciences, or related field* At least 1-2 years of relevant experiences in clinical trial coordination, IRB submissions, or patient-facing research (entry-level candidates with strong interest are welcome to apply)* Familiarity with biospecimen collection and handling, molecular biology, or omics techniques* Good written and oral communication skills* Proficiency in data management, statistical analysis, or clinical research sofeware* Strong organizational and project management skills* Excellent interpersonal skills to work both independently and collaboratively within a multidisciplinary team* Demonstrated interest in integrative medicine, oncology, or translational researchThe College of Science seeks a diverse and inclusive workforce and is committed to equality of opportunity. We welcome applications from all and recruit on the basis of merit, regardless of age, race, gender, religion, marital status and family responsibilities, or disability.We regret to inform that only shortlisted candidates will be notified.Hiring Institution: NTUNTU is also home to world-class autonomous institutes – the National Institute of Education, S Rajaratnam School of International Studies, Earth Observatory of Singapore, and Singapore Centre for Environmental Life Sciences Engineering – and various leading research centres such as the Nanyang Environment & Water Research Institute (NEWRI) and Energy Research Institute @ NTU ( ).Ranked amongst the world’s top universities by QS, NTU has also been named the world’s top young university for the past seven years. The University’s main campus is frequently listed among the Top 15 most beautiful university campuses in the world and has 57 Green Mark-certified (equivalent to LEED-certified) buildings, of which 95% are certified Green Mark Platinum. Apart from its main campus, NTU also has a campus in Novena, Singapore’s healthcare district.Under the NTU Smart Campus vision, the University harnesses the power of digital technology and tech-enabled solutions to support better learning and living experiences, the discovery of new knowledge, and the sustainability of resources.For more information, visit
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