265 Pharmaceutical Specialist jobs in Singapore

We are seeking a skilled Pharmaceutical Specialist to provide high-quality dispensing services and pharmaceutical care to patients.

• Deliver exceptional patient care through quality dispensing services and pharmaceutical advice
• Provide Outpatient Pharmacy Services, including medication review and anticoagulation services
• Counsel patients on medications and provide information to healthcare professionals, handling public inquiries

To succeed in this role, you will require:

• Possess a Degree in Pharmacy and be a Registered Pharmacist with the relevant authority
• Demonstrate initiative and ability to work independently
• Exhibit excellent interpersonal and communication skills

Benefits of Working as a Pharmaceutical Specialist:

You will have the opportunity to work in a dynamic environment, delivering exceptional patient care and contributing to the well-being of our community. If you are a motivated and compassionate individual with a passion for pharmacy, we encourage you to apply for this rewarding role.

**Job Summary:** The role of a pharmacist entails dispensing medications accurately, monitoring drug interactions, and collaborating with healthcare professionals to develop patient care plans. Medication safety is a top priority.

We are seeking a registered pharmacist with relevant experience in clinical or hospice settings. The ideal candidate will possess strong attention to detail and up-to-date knowledge of drug regulations and best practices.

Key responsibilities include:

• Accurately dispense medications and monitor drug interactions
• Collaborate with healthcare professionals to develop patient care plans
• Maintain accurate records and adhere to regulatory guidelines

The successful candidate will be a team player who can work effectively in a fast-paced environment. They will also have excellent communication skills and the ability to work well under pressure.

Benefits:

• A competitive salary package
• A comprehensive benefits program
• Ongoing training and professional development opportunities

This is an exciting opportunity for a dedicated and motivated individual to join our team as a pharmacist. If you are passionate about delivering high-quality patient care and have a strong commitment to excellence, we encourage you to apply.

Job Overview:

We are seeking a highly skilled and dedicated Nurse to join our organization, playing a pivotal role in the treatment and education of patients.

The ideal candidate will be responsible for identifying at-risk patients, providing personalized care and support, and ensuring all tasks are completed efficiently.

• Handling patients in basic treatments
• Providing patient education on disease progress and self-management techniques
• Tracking patient outcomes and data

To succeed in this role, the successful applicant must possess a Diploma in Nursing from a recognized institution and be registered with the relevant nursing authority.

This role offers the opportunity to work with a talented team, make a meaningful contribution to patient care, and advance your career as a professional nurse.

Job Description

In this role, you will be responsible for providing support to healthcare professionals by ensuring the accurate dispensing of medication to patients.

Key responsibilities include managing the inventory of cardiovascular drugs, maintaining a clean and organized work environment, and collaborating with the nursing team to oversee drug stock take and discrepancies.

Additional duties will involve reviewing bonus tier schemes, monitoring key pharmaceutical contacts, and providing regular updates on medication purchases and stock movement.

The ideal candidate should possess excellent communication skills and have a strong understanding of pharmaceutical practices. A minimum diploma in Pharmaceutical Science is also required.

Required Skills:

• Excellent communication skills


• Strong organizational and time management skills


• Ability to work accurately and efficiently in a fast-paced environment


• Basic knowledge of pharmaceutical principles and practices

Benefits:

• Competitive salary and benefits package


• Opportunities for professional growth and development


• Collaborative and dynamic work environment

How to Apply:

Interested candidates should submit their application, including a cover letter and resume, to the relevant department.

Company description:

SingHealth Polyclinics, a leader in family medicine, provides seamless, patient-centred and preventive healthcare that is affordable and accessible to all. SingHealth Polyclinics' network of polyclinics provides primary healthcare services to the community. It plays an integral role in promoting a healthy lifestyle within the community and empowering families with the knowledge of common health issues, care and treatment options. SingHealth Polyclinics is a member of Singapore Health Services (SingHealth) - a public healthcare cluster which also manages three hospitals and five specialty centres.

Job description:

Job Description

You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.

Requirements:

• Life Science or Nursing Degree holder. Candidates with Nursing Diploma must have minimum 2 years of relevant experience
• At least 1-2 years of experience in clinical research coordination
• Ability to converse in mainstream languages (able to speak in local dialects will be an added advantage) to handle patient queries on the research study
• Strong organizational skills, able to work independently and/or a team player, meticulous in details
• Proficient with MS Office applications

You will be part of the research team involved in various clinical projects and will be required to perform the following:

• Act as a liaison between study participants and the research team; provide study participants with clear explanation of purpose of study and assist with obtaining informed consent

• Schedule participants for visits to clinic for the required tests and evaluations, collect their samples and assist in monitoring the participants' well-being

• Assist with compilation and management of patient data; ensure study is conducted in compliance with study protocols, established procedures and timeline

• Draft reports for submission to the relevant authorities

• Tabulate and document financial payments received or made to the study

Job Requirements:

• Bachelor's Degree in Nursing/ Medical Technology / Health Science / Life Science / Pharmacy
• Proficient in Microsoft Office Applications

The Laboratory of Surgical System & Service Innovation (3SI) is a multi-disciplinary laboratory that provides a platform for cutting-edge surgical health services research that informs healthcare systems, policies, and programs to provide high-value, patient centered care for patients and their families undergoing surgery.

We are looking for an enthusiastic, dynamic, meticulous, and responsible Research Coordinator to work closely with a team of experienced researchers and the clinical team in health system, services innovation, and novel surgical technologies research. You will be part of a holistic clinical and health services research team whose mission is to improve clinical outcomes for seriously ill patients undergoing major surgery.

Responsibilities:

• Patient recruitment & consent
• Data Collection, Management, Analysis
• Research Grant support
• Prepare and submit IRB applications, amendments, continuing reviews, and study closures
• Administrative Support (eg. Process claims, reimbursements, and invoices for team members)
• 1 year experience in research administration, IRB-related work and patient consenting required
• Any ad hoc duties required

Job requirements:

• Bachelor's degree in a relevant field (e.g., life sciences, public health, research administration, nursing, ethics)
• Fresh grads are welcome to apply
• Interest in scientific research and willing to engage in various aspects of the research processes
• Proficient computer knowledge (MS Office – Word, Excel, PowerPoint)
• Good interpersonal skills

Salary: up to $4000

Duration: 6 months contract

Working Days & Hours: Mon-Fri Office Hours

Location: Jurong

Job Description:

Subject Recruitment and follow up

• Be involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms.
• Obtain consent taking, administer study questionnaires and follow-up on study participants.
• Work closely with research team, clinicians, clinic staff and other relevant internal departments to ensure research study needs are met.
• Able to work on tight timelines, set sensible targets and achieve research deliverables.

Research Documentation / Administrative duties

• Conduct research study activities like patient recruitment, data collection and data management.
• Assist in data collection from electronic health records.
• Set up and maintain study investigator files, including records of consent taken and blood collection.
• Maintain study records in databases such as Redcap and in electronic health record systems.
• Responsible for maintaining strict adherence to research protocols i.e., HBRA.
• Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.
• Prepare necessary documentation for audit purposes.
• Coordinate the submission of new IRB applications, study amendments and annual reports.
• Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.
• Assist with any other duties of a similar nature that are delegated by the PI.

Job Requirements: Min Degree in Life Sciences or similar

Interested candidates, please submit your resume to:

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R

The SINGAPORE EYE RESEARCH INSTITUTE (SERI) serves as Singapore's national research institute for ophthalmic and vision research. SERI functions as the research arm of the various clinical ophthalmic centres in Singapore including the Singapore National Eye Centre, the National University Health Systems (NUHS), Tan Tock Seng Hospital etc., and further works in collaboration with Duke-NUS Graduate Medical School and various biomedical research institutions, as well as major eye centers and research institutes throughout the world. SERI has developed a world-leading reputation in broad-based clinical translational research and epidemiological programmes for many eye diseases, particularly disease relevant to Asia. SERI currently has close to 200 staff with an annual budget of $20M.

Clinical A/Prof Anna CS Tan is a Principal Investigator working in medical retina conducting study that is focused on studying patient-centered outcomes and methods to improve patient's adherence to long term treatment for chronic retinal diseases. She is inviting passionate, committed candidates interested in improving patient care for the position of Clinical Research Coordinator (CRC).

Position Summary

As a CRC, you will execute best practice clinical research to support quantitative and qualitative data collection to help assess patient reported outcomes and implement interventions aimed at improving adherence to treatment and follow up for chronic eye diseases. You will be involved in the planning, development, and oversight of the day-to-day clinical activities for specified clinical research initiatives, as established by the principal investigator (PI) You will be expected to provide support for an array of duties related to the various study protocol, including recruitment of English and Mandarin-speaking study subjects, case notes extraction, questionnaire administration, and managing the study sample database. You will also develop and administer budgets and operating procedures for the project, coordinating day-to-day administration related interactions with associated departments, agencies, and vendors. Flexibility to work on multiple projects sharing similar protocols, a natural aptitude for organization, and being deadline-driven are important attributes for this dynamic position.

Job Description

• Plan, schedule and carry out day-to-day study procedures such as recruitment of participants and collection of high quality clinical and patient-related data
• Following training and validation, conduct refraction, administer questionnaires, and carry out other clinical procedures as specified within the relevant study protocols
• Prepare various study materials (invitation letters, brochures, screening log forms, etc.).
• Ensure that all clinical activities are carried out in accordance with established research protocols and in compliance with applicable laws, regulations, policies, and procedural requirements
• Undertake data entry and preparation of reports to share the study status (e.g., recruitment etc.,) with the supervisor
• Serve as the primary point of liaison between investigators, ancillary departments, regulatory bodies, and research participants
• Perform other job-related duties, as assigned

Requirements

• Diploma/degree in Optometry, Social Sciences, Psychology, or other health or science-related disciplines
• Strong communication (especially spoken and listening) and interpersonal skills, leadership, and people management skills
• Excellent organizational and analytical skills with project management experience
• Experience administering survey questionnaires and collecting clinical data from study participants
• Computer competency including proficiency in MS Office (Word, Excel, PowerPoint)
• Ability to manage multiple projects simultaneously and effectively work in teams
• Have a pleasant and engaging demeanour
• Able to work from Mondays to Fridays and on alternate Saturdays. Might be required to work after-office hours (only when required for certain occasions).
• Candidates without experience are welcome to apply

Preferred

• Experience working with a wide variety of stakeholders (patients, doctors, nurses, researchers, admin staff etc.) and ability to manage group dynamics effectively