472 Healthcare Project Management jobs in Singapore

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.

We are seeking skilled nurses to conduct clinical trials and provide nursing care.

• Screen study participants according to regulatory guidelines and ethical standards
• Conduct informed consent discussions and monitor patient progress
• Administer study-related interventions, including medications and treatments
• Perform assessments and follow-ups with participants

Requirements:

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

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.

The Senior Clinical Trials Specialist plays a pivotal role in the successful execution of clinical trials. This role oversees and ensures that all trials are conducted and documented according to the established protocol, regulatory requirements, Good Clinical Practice Guidelines, and standard operating procedures.

• Develop and implement strategic plans for effective subject recruitment.
• Maintain open communication with cross-functional teams regarding subject screening and recruitment rates.
• Ensure prompt response to inquiries within 10 working days.
• Cultivate strong relationships and facilitate collaboration across departments to enhance operational efficiency.
• Optimize invoicing processes to minimize payment delays.

• Bachelor's degree in Nursing, Medicine, Pharmacy, or related fields, preferably with experience in clinical trials or research.
• 1-2 years of experience in conducting clinical trials, particularly in Hematology/Oncology interventional trials.
• Familiarity with setting up cell therapy trials.
• ICH GCP training.
• Strong organizational and time management skills.
• Effective communication and interpersonal skills.
• Independent learning ability.
• Collaborative mindset with excellent team player qualities.

Job Overview

Clinical trials play a crucial role in advancing medical research and improving patient care. As a nursing clinical trials specialist, you will be responsible for ensuring the smooth conduct of these trials.

You will work closely with cross-functional teams to implement regulatory guidelines and ethical standards. This involves conducting informed consent discussions, monitoring patient progress, and collecting data during clinical trials.

Key responsibilities include:

• Screening study participants according to regulatory guidelines
• Conducting assessments and follow-ups with participants to address concerns and provide education
• Administering study-related interventions as per protocol

Requirements

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

Benefits

As a nursing clinical trials specialist, you will have the opportunity to work on cutting-edge medical research and make a meaningful contribution to the healthcare industry. You will also have access to ongoing training and development opportunities to enhance your 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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As a healthcare professional, you will play a vital role in the success of our clinical trials. We are seeking dedicated and skilled individuals to join our team as study coordinators.

Key Responsibilities:

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

To be successful in this role, you will need:

• A degree in a healthcare-related field (e.g., nursing, medicine).
• Experience working in clinical trials or a related field.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Attention to detail and organizational skills.

We offer a competitive salary and benefits package, including:

• Opportunities for career growth and professional development.
• A supportive and collaborative work environment.
• The chance to contribute to groundbreaking research and make a difference in people's lives.

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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