Clinical trial scientist
2 weeks ago
Based in Basildon (hybrid role: 3 days office, 2 days home per week) Clinical Trial Scientist Salary: Competitive + Benefits + Bonus Permanent or FTC role If you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you. Join us to help improve peoples’ lives and make healthcare better for everyone Why Pharmanovia? Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines. Our core behaviours are: We keep our promises and do as we say. We value our heritage and foster an entrepreneurial spirit. We reinvest in our future – in our products, our brands, and our people. We give back to our communities. Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U. A. E., India, Singapore, Italy, Spain, and South Korea. We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About the role: Reporting to Head of Clinical Development, you will play a key role in the design, execution, and oversight of clinical trials across various phases (I-IV). This position collaborates with cross-functional teams, including Regulatory Affairs, Market Access, Strategic Marketing, Legal and Medical Affairs, to ensure scientific integrity and operational excellence in clinical trial planning and execution. You will contribute to protocol development, data analysis, and scientific communication to drive clinical development strategies and achieve high-quality outcomes that meet regulatory and corporate standards. You will also act as the main point of interaction with external CROs, help in identifying best partners to appoint for trial execution and support, as well as ensuring each clinical study protocol is designed with scientific integrity with the endpoints clearly addressing the study objectives in line with the CDP and business needs and other regulatory standards of all trials including IITs. The department has an ethos of continuous improvement, refining systems and creating efficiencies. This, along with the rapid growth of the business, leads to a varied and dynamic working environment. Main responsibilities and duties: Clinical Trial Design: Develop and contribute to the design and writing of clinical trial protocols, investigator brochures, and related study documents. Collaborate with the clinical development team to establish study objectives, endpoints, and inclusion/exclusion criteria. Provide scientific input into trial design, statistical analysis, and risk management strategies. Study Execution and Oversight: Ensure trials are conducted in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. Oversee data collection, quality control, and data integrity throughout the trial lifecycle. Serve as a point of contact for clinical trial sites, supporting trial-related activities, troubleshooting, and monitoring patient safety. Data Analysis and Reporting: Analyse and interpret clinical data, working closely with biostatistics and data management teams to ensure data accuracy. Contribute to the preparation of clinical study reports (CSRs), abstracts, posters, and manuscripts for internal and external presentations. Review study results for accuracy and consistency, identifying key findings relevant to product development. Cross-Functional Collaboration: Partner with Medical Affairs, Regulatory Affairs, Market Access, and Pharmacovigilance to ensure alignment on study objectives and milestones. Provide scientific expertise in meetings with key stakeholders, including regulatory bodies, investigators, and partners. Contribute to project timelines, budget adherence, and risk management. Regulatory Support: Assist in the preparation of regulatory submissions, including PIP and MAAs, by providing scientific insights and data. Stay current with regulatory guidelines, therapeutic area trends, and competitive landscape to inform clinical development strategies. About you – what you will need to have: Advanced degree (Ph. D. or equivalent) in life sciences, clinical research, or related field. Minimum 5+ years of experience in clinical trial management. High level of scientific and analytical ability to design and interpret complex clinical studies. Ability to work cross-functionally and foster strong partnerships within and outside the organization. Strong attention to protocol adherence, data accuracy, and scientific integrity. Effective problem-solving skills, with a proactive approach to identifying and addressing trial challenges. Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements. Excellent communication and presentation skills, with an ability to translate complex scientific information for diverse audiences. Determined, driven to achieve results and business minded. Proven track record of working and leading a cross-functional team in a matrix environment. The ability to review both data and procedures in detail and the ability to see the greater overall picture. What we offer: We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working. By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible. Apply now and become part of our team #J-18808-Ljbffr
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Clinical Trials Specialist
18 hours ago
Singapore ICON CLINICAL RESEARCH (PTE) LIMITED Full timeAbout 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...
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Clinical trial scientist
2 weeks ago
Singapore Pharmanovia Full timeBased in Basildon (hybrid role: 3 days office, 2 days home per week)Clinical Trial ScientistSalary: Competitive + Benefits + BonusPermanent or FTC roleIf you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you. Join us to help improve peoples’ lives and...
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Clinical trials associate
3 weeks ago
Singapore IQVIA LLC Full timeClinical Trials Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1452762This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA. In this role, you will be involved in the process of supporting clinical trials for various...
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Clinical trials associate
3 weeks ago
Singapore IQVIA LLC Full timeClinical Trials Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1452762 This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA. In this role, you will be involved in the process of supporting clinical trials for various...
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Clinical Trial Coordinator
3 weeks ago
Singapore MEDPACE Full timeMedpace 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...
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Clinical Trials Specialist
5 days ago
Singapore NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD Full timeJob SummaryWe are seeking a skilled Clinical Trials Specialist to join our team at the National Cancer Centre Singapore. The successful candidate will be responsible for reviewing and finalizing clinical trial contracts, working closely with the SingHealth Legal Department to negotiate agreement terms with commercial sponsors, CROs, academic institutions or...
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Clinical trial manager
2 weeks ago
Singapore Pharmanovia Full timeBased in Basildon (hybrid role: 3 days office, 2 days home per week) Clinical Trial Manager Salary: Competitive + Benefits + Bonus Permanent or FTC role If you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you. Join us to help improve peoples’ lives...
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Manager (Clinical Trial - Contracts)
6 months ago
Singapore NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD Full timeRoles & ResponsibilitiesWe are looking for a Manager with sufficient professional experience and stature to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore. The role will mainly assist our Clinical Trials Office to review and finalize contracts related to clinical trials...
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Clinical trial manager
2 weeks ago
Singapore Pharmanovia Full timeBased in Basildon (hybrid role: 3 days office, 2 days home per week)Clinical Trial ManagerSalary: Competitive + Benefits + BonusPermanent or FTC roleIf you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you. Join us to help improve peoples’ lives and...
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Senior Clinical Trials Specialist
3 days ago
Singapore NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD Full timeJob 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...
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Clinical Research Coordinator
3 months ago
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Clinical Trial Operations Specialist
18 hours ago
Singapore RECRUIT EXPRESS PTE LTD Full timeAt 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...
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Clinical Trial Coordinator
5 days ago
Singapore TUM CREATE LIMITED Full timeRoles & 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...
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Clinical trial manager
4 weeks ago
Singapore Medpace, Inc. Full timeJob Summary Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials....
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Clinical Trials Assistant
6 hours ago
Singapore IQVIA Full timeJob Responsibilities: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution,...
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Singapore ProZ Full timeWe are seeking an experienced Clinical Trials translator to work on our projects in Singapore. As a key member of our team, you will be responsible for translating clinical trial documents from English to Brazilian Portuguese.Job Description:We are looking for qualified translators with expertise in the pharmaceutical industry, particularly in Clinical...
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Clinical Trials Translation Specialist Wanted
3 weeks ago
Singapore ProZ Full timeClinical Trials Translation and Editing OpportunityJob posted at: Our Singapore location (GMT: )Job type: Translation/editing/proofing jobServices required: Translation, Checking/editingJob Description:We are seeking a qualified Clinical Trials Translation Specialist for our projects in Singapore. As a member of our team, you will be responsible for...
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Senior Clinical Trial Specialist
3 days ago
Singapore TUM CREATE LIMITED Full timeAre you passionate about supporting a clinical trial that optimizes light exposure for senior citizens? We are seeking a highly motivated and detail-oriented Clinical Trial Coordinator to join our dynamic research team at TUMCREATE LIMITED in Singapore.About the RoleThe successful candidate will play a crucial role in the implementation and progress of our...
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Clinical Trials Translation Specialist
2 weeks ago
Singapore ProZ Full timeJob Title: Clinical Trials Translation Specialist - Competitive RatesAbout the JobWe are seeking a highly skilled Clinical Trials Translation Specialist to join our team at ProZ. This is a unique opportunity to work on a variety of clinical trials related projects, leveraging your expertise in translation, editing, and proofreading.Job DescriptionThe...
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Clinical Trial Coordinator
6 hours ago
Singapore TUM CREATE LIMITED Full time $4,000 - $4,500About 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 www.tum-create.edu.sg for...
