Clinical Trial Manager - Remote Opportunity with pfm

Join pfm as a Clinical Trial Manager where you will play a vital role in overseeing clinical trials from conception to completion. In this remote position, you will collaborate with cross-functional teams to ensure that all studies are conducted according to regulatory guidelines and within timelines.

Join our dynamic team at Precision Medicine Group as a Clinical Trial Manager and play a pivotal role in advancing innovative healthcare solutions. In this fully remote position, you will lead and oversee clinical trial operations, ensuring adherence to regulatory guidelines and protocol compliance.

Join pfm as the APAC Startup Lead, where you will spearhead initiatives to foster innovation and growth in the Asia-Pacific region. In this pivotal role, you will collaborate with cross-functional teams and leverage your expertise to drive strategic partnerships and enhance our market presence. We are looking for a dynamic individual with a passion for startups and a proven track record in leadership.

Job Title: Clinical Project Lead - VaccinesLocation: Singapore/Malaysia/Vietnam/the Philippines/China (Remote)Reports To: Head, Global Clinical OperationsEmployment Type: Full-TimeAbout UsAt fuku, we are at the forefront of biopharmaceutical innovation, committed to developing life-saving vaccines and therapeutics. As we broaden our global reach, we are looking for a seasoned Clinical Project Manager to spearhead clinical trial execution across Southeast Asia, aligning with our ambitious international growth plans.The Opportunity- Take the lead in transformative vaccine trials across various Southeast Asian markets.- Benefit from the flexibility to work from Singapore, Malaysia, Vietnam, the Philippines, or China.- Ensure comprehensive study delivery from initiation through to close-out.- Collaborate with cross-functional teams to advance our portfolio in infectious diseases.Key Responsibilities- End-to-End Project Leadership: Direct and oversee regional operational strategy, timelines, budgets, and risk mitigation for Phase II-IV vaccine trials spanning Southeast Asia (Singapore, Malaysia, Thailand, Indonesia, Vietnam, Philippines).- Site Excellence: Manage site selection, initiation, monitoring, and close-out, ensuring full compliance with ICH-GCP and local regulations.- Vendor Partnership: Lead CROs, central labs, and regional vendors to ensure timely delivery of quality data.- Stakeholder Engagement: Act as the primary contact for investigators, internal teams (Medical, Regulatory, Data Management), and country managers.- Risk Management: Proactively identify and address operational challenges across diverse regulatory environments.- Resource Stewardship: Oversee regional budgets up to $[X]M and provide mentorship to junior CRAs.Required Qualifications- Experience: Minimum of 5 years in clinical operations with at least 2 years of direct project management experience in multi-country trials.- Therapeutic Expertise: Proven experience in vaccine clinical trials (prophylactic vaccines required; COVID, influenza, RSV, etc.).- Progression Path: Senior/Lead CRA or CRA II poised for project leadership, with a record of increasing responsibility.- Regional Knowledge: Successful track record of managing studies in Southeast Asia; familiarity with country-specific regulatory frameworks.- Technical Skills: Proficient in ICH-GCP, clinical trial management systems (CTMS), and risk-based monitoring.- Education: Bachelor's degree in Life Sciences (advanced degree preferred).- Language: Business fluency in English; proficiency in Chinese is advantageous.

Precision for Medicine is a renowned Clinical Research Organization, uniquely positioned to advance the field of precision medicine. Our integrated services combine innovative clinical trial designs, leading operational and medical expertise, advanced biomarker and data analytics solutions, and a genuine commitment to addressing rare diseases and oncology, alongside other therapeutic domains.As we expand our operations, we are looking for an enthusiastic Associate Director of Compensation & Benefits to become an integral part of our dynamic team.Job Summary:The Associate Director of Compensation & Benefits will oversee the implementation and management of our international compensation and benefits initiatives. This role involves conducting detailed analyses and providing strategic insights into the organization’s compensation and benefits framework. The successful candidate will participate in international salary surveys, ensuring competitive benchmarking, and collaborate closely with HR Business Partners, Talent Acquisition, Finance, Legal, and Business Leaders to maintain market competitiveness, uphold internal equity, and ensure compliance across all regions. Additionally, this role will support the annual compensation planning processes, including merit, promotions, and bonuses, as well as manage all international benefit plans and related administration.

Join our esteemed client, a premier healthcare provider in Singapore, committed to delivering outstanding patient care and pioneering medical solutions. As a Clinic Manager, you will play a crucial role in overseeing the clinic's daily operations, ensuring top-notch service delivery and operational excellence. Your key responsibilities will include:- Managing clinic staff through effective hiring, training, scheduling, and performance evaluation processes.- Crafting and implementing policies and procedures aimed at enhancing patient care and operational efficiency.- Monitoring the financial performance of the clinic, including budgeting, billing, and revenue management.- Ensuring adherence to healthcare regulations and standards.- Collaborating with medical staff to optimize patient care and clinic services.- Actively addressing patient concerns and feedback to elevate service quality.- Coordinating with external partners and vendors to support clinic operations.- Preparing and presenting performance reports to senior management.We are looking for candidates who meet the following requirements:- A Bachelor's degree in healthcare administration, business management, or a related field.- A minimum of 3-5 years of experience in a healthcare management role.- Strong leadership and team management capabilities.- Excellent communication and interpersonal skills.- Proficiency with healthcare management software and systems.- Comprehensive knowledge of healthcare regulations and compliance standards.- The ability to multitask and prioritize effectively in a fast-paced environment.- Strong problem-solving and decision-making skills.As part of our team, you will enjoy a range of benefits including:- A competitive salary complemented by performance-based bonuses.- Comprehensive health, dental, and vision insurance.- A retirement savings plan with company matching.- Paid time off and holidays.- Opportunities for professional development and continuing education.- Employee wellness programs.- A supportive and collaborative work environment.

Join Intuitive Surgical as a Senior Manager in Regional Clinical Marketing for Asia, where you will play a pivotal role in driving our clinical marketing strategies across diverse markets. You will collaborate closely with local marketing teams, clinical specialists, and sales personnel to develop and implement effective marketing initiatives that highlight the benefits of our innovative surgical systems.

Join our innovative telehealth platform, 'Intellect', as a Clinical Provider focused on empowering clients' mental health and personal growth tailored to their unique needs. You will conduct engaging 60-minute video sessions to provide essential support and guidance.This freelance opportunity allows you to set your own hours, offering flexibility to enhance your current practice or job. While preference is given to local candidates, we welcome applications from others as well. Be part of a committed community of Clinical Psychologists and Counsellors dedicated to broadening mental health access and offering effective mental health coaching.

Join Prestige Biopharma Limited as a Clinical Quality Intern and immerse yourself in the dynamic world of biopharmaceuticals. In this role, you will support our clinical quality assurance efforts, ensuring that all processes align with industry standards and regulations. This internship offers a unique opportunity to work closely with experienced professionals in the field, gain practical insights, and contribute to the advancement of innovative therapies.

Join our dynamic team at Intellect HQ as a Clinical Psychologist! We are on the lookout for a dedicated and skilled professional who excels in providing evidence-based therapeutic interventions. The right candidate will possess extensive experience in Cognitive Behavioral Therapy (CBT) and be adept at conducting neuropsychological assessments for individuals across various age groups, including youth, adolescents, and adults. Your proficiency in report writing will also be essential in this role.Key Responsibilities: Craft and execute tailored treatment plans leveraging evidence-based strategies with an emphasis on CBT. Facilitate individual, couples, and group therapy sessions, available both in-person and through virtual platforms. Administer neuropsychological assessments for conditions such as ADHD, dyslexia, and other learning challenges. Engage in team meetings and contribute to the advancement of service delivery and improvement initiatives. Work collaboratively with our interdisciplinary team to formulate and implement client-centered treatment approaches. Coordinate closely with our 24/7 helpline responders to manage client risk and ensure safety during crises. Maintain thorough and accurate client records in compliance with professional and legal standards. Stay abreast of developments in the field through ongoing professional education and training. Flexibly commit to clinic hours, operating Monday to Friday from 10am to 9pm, and Saturdays from 10am to 2pm, including two evening shifts and two Saturdays each month. Requirements:A Master's Degree in Clinical Psychology.A minimum of 3 years of clinical experience post-graduation, ideally within a mental health context.Proficient in both individual and group therapy facilitation.Adept in organizing and executing online seminars using various digital platforms and capable of creating engaging content.Experience in effectively managing crisis situations.Familiarity with administering psychological assessments.Demonstrated expertise in providing evidence-based treatments, particularly CBT.Current registration or eligibility for registration as a Clinical Psychologist with the Singapore Psychological Society (SPS).Willingness to conduct in-person sessions at our office or partner locations.Preferred: Experience offering clinical supervision to fellow mental health professionals.Key Attributes: Exceptional interpersonal and communication abilities. Compassionate and empathetic approach to client care. Collaborative skills and effectiveness in a multidisciplinary team setting. Strong commitment to evidence-based practice.

As a Medical Director at fuku, you will play a pivotal role in steering medical and scientific leadership for our clinical trials and research initiatives. Your responsibilities will include:- Leading the development and critical review of clinical trial protocols, investigator brochures, and other essential study documents.- Ensuring that all medical operations align with regulatory mandates, ethical standards, and the company’s internal policies.- Collaborating closely with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to guarantee the successful execution of projects.- Acting as the primary medical liaison for clients, investigators, and regulatory bodies.- Providing medical oversight throughout the clinical trials, focusing on safety monitoring and data analysis.- Engaging in business development efforts by offering medical insights during client meetings and proposal preparations.- Staying abreast of industry developments, therapeutic innovations, and regulatory updates to guide strategic planning.- Mentoring and developing the clinical and medical team to boost overall performance and capabilities.- Supporting the publication of clinical trial findings in scientific journals and presenting at industry conferences.

psicro is hiring a Medical Monitor with board certification in Internal Medicine to join the team in Singapore. This role centers on overseeing clinical trials, with a strong emphasis on regulatory compliance and patient safety at every stage of research. What you will do Supervise clinical trials to ensure all activities follow regulatory requirements and established protocols Monitor patient safety and address clinical issues as they occur Collaborate with multidisciplinary teams to help achieve research objectives Provide medical expertise for both the design and execution of trials Location This position is based in Singapore.

Role OverviewResponsibilities: Join our dynamic Medical Communications team as a Medical Writer, focusing on the strategic planning and creation of scientific publications. Your role will entail comprehensive analysis and innovative communication of clinical trial data, producing abstracts, posters, oral presentations, and manuscripts for submission to esteemed scientific journals and conferences. You will collaborate with a diverse array of clients, including leading pharmaceutical and medical technology firms, health organizations, and charitable institutions.Salary: S$4,500 per monthBenefits: Enjoy hybrid working options, a generous holiday allowance, flexible working hours, private medical insurance, extensive travel insurance, complete funding for external training, and more.Role Type: Full-time, permanentStart Date: We are currently looking for candidates for roles starting in 2026.Location: Successful candidates will be based in our Singapore office.About the PositionThis role is perfect for those with a background in scientific research or recent graduates eager to join a thriving team. You will work in our Singapore office as part of the Asia-Pacific team, collaborating closely with colleagues from our UK and US teams.As a Medical Writer, you will engage in projects that involve detailed data analysis from clinical trials and the creative presentation of this analysis in various formats, including posters, slide decks, value dossiers, reports, and peer-reviewed publications. These deliverables are essential for our clients as they communicate with external stakeholders crucial to the successful adoption of innovative therapies. Your work will be organized on a project-by-project basis, often involving multiple projects across different disease areas simultaneously.You will collaborate with experienced colleagues in Singapore, the UK, and the US who will provide personalized training in the technical aspects of the role, including project management and effective client communication. Successful project delivery will demand close cooperation with clients, and after a successful onboarding period, you will gradually participate in teleconferences and face-to-face meetings with external stakeholders.We welcome applications from both entry-level candidates and those with prior experience. We are seeking ambitious individuals who are...

As a Clinical Sales Specialist at Eurofins Scientific, you will play a crucial role in driving sales of our innovative laboratory services and solutions. You will be responsible for building and maintaining relationships with healthcare professionals, laboratories, and other stakeholders to promote our comprehensive range of services. Your ability to understand client needs and provide tailored solutions will be essential in achieving sales targets and expanding our market presence.

Join GitLab as an Ecosystem Sales Manager and play a pivotal role in driving growth through strategic partnerships and sales initiatives. In this fully remote position, you'll collaborate with cross-functional teams to enhance our ecosystem and achieve ambitious sales targets.

Join Prestige Biopharma Limited as a Clinical Operations Intern, where you will gain hands-on experience in the biopharmaceutical industry. This internship offers a unique opportunity to work closely with our clinical operations team and support the execution of clinical trials. You will learn about the processes involved in clinical study management and contribute to critical projects that advance our mission of developing innovative therapies.

Join Modern Health as a Client Success ManagerModern Health is a pioneering mental health benefits platform designed for employers, offering a comprehensive global solution that provides employees with access to personalized mental health resources. Our platform supports various aspects of well-being, including emotional, professional, social, financial, and physical health, ensuring that individuals can manage their mental health effectively. Whether addressing stress or more serious conditions like depression, Modern Health is dedicated to guiding individuals toward the appropriate care at the right moment. We aim to empower all employees to be their best selves, meeting them at every step of their mental health journey.With backing from prominent investors such as Kleiner Perkins, Founders Fund, John Doerr, Y Combinator, and Battery Ventures, we have successfully raised over $170 million in under two years, establishing Modern Health as the fastest female-founded company in the U.S. to achieve Unicorn status.When you join our team, you can expect a vibrant culture defined by:“It Takes a Village” culture: We prioritize high empathy and accountability, striving to unite top talent in our industry to achieve ambitious goals that make mental health a priority.Obsessed with Winning: Our team is driven, ambitious, and passionate about delivering excellence while continually innovating to meet our customers’ needs.Accountability: We function as a cohesive team, promoting transparent communication and continuous feedback to foster trust and growth.Empathy: Our supportive and diverse culture encourages collaboration, respect, and a willingness to support one another in achieving our lofty objectives.Bias Towards Action: In our fast-paced environment, we encourage initiative, decision-making, experimentation, and iteration.Modern Health operates remotely, embodying a hyper-growth mindset and has gained recognition for its excellence, winning multiple awards.

About Heidi HealthHeidi Health is revolutionizing the healthcare landscape with our AI Care Partner, designed to assist clinicians throughout their workflow, from documentation to patient care delivery.Our mission is to enhance healthcare capacity while ensuring that care remains deeply human. In just 18 months, we have reclaimed over 18 million hours for clinicians and facilitated more than 73 million patient visits. Presently, Heidi is empowering over two million patient visits weekly across 116 countries and in over 110 languages.Founded by healthcare professionals, our team combines the expertise of clinicians, engineers, designers, scientists, and creatives, all dedicated to fostering the human connection at the core of healthcare.With nearly $100 million in funding, Heidi is expanding its footprint in the USA, UK, Canada, and Europe, collaborating with leading health systems such as the NHS, Beth Israel Lahey Health, MaineGeneral, and Monash Health.We prioritize rapid innovation while remaining anchored in proven methodologies, shaping the future of healthcare. Are you ready to join us in this exciting journey?Your RoleAs a Clinical Associate, you will play a critical role in supporting our clinical AI products for clients based in Japan. Your responsibilities will include creating detailed and precise document templates for our users, as well as producing engaging written and video content for our website.You will collaborate closely with our Medical Knowledge and Business teams to ensure user success.Key Responsibilities:Utilize your clinical expertise to design and customize specialized note and document templates as requested by clinicians and the Medical Knowledge & Business teams.Convert clinical notes and documentation provided by our users into expertly crafted templates compatible with Heidi.Work with users to optimize and refine their existing templates to meet their needs effectively.Create content for our website and record short videos showcasing the diverse applications of Heidi’s templates for clinicians in various settings.Develop an in-depth understanding of our product and its utilization by clients in their practices.Deliver outstanding customer support and engagement to ensure user satisfaction with our products.

Company OverviewFounded in 2019, Shanghai Spectrumedics Medical Technology Co., Ltd. (SPECTRUMEDICS) is a pioneering medical technology firm dedicated to the research, development, manufacturing, and global commercialization of cutting-edge interventional cardiovascular devices. Our expertise lies in creating minimally invasive solutions for vascular calcification. The Sonico-CX® Coronary Intravascular Shock Wave Therapy (IVL) System, our flagship product, proudly holds the distinction of being the first shock wave device in China to secure both NMPA and CE certifications. With a robust presence in both Shanghai and Singapore, we uphold stringent manufacturing compliance, possess multiple patents, and are actively expanding our global clinical and commercial reach.Position SummaryThe Clinical Support Specialist plays a crucial role in delivering hands-on clinical support, training, and education for the Sonico-CX® IVL system. This position collaborates closely with physicians, cath lab personnel, distributors, and internal teams to ensure the safe and effective use of devices, facilitate therapy adoption, and gather valuable real-world clinical feedback. This role is field-oriented and case-focused, necessitating in-person clinical assistance, on-call availability, and tight collaboration with distributor and clinical partners.Main ResponsibilitiesClinical Support & TrainingProvide immediate, hands-on clinical assistance during IVL procedures to guarantee optimal and safe device usage.Assist clinicians in system setup, catheter preparation, imaging workflows, and device delivery.Conduct structured training sessions for physicians, nurses, cath lab staff, and internal field teams.Offer remote clinical support through on-call conference calls for urgent distributor-assisted cases.Train and certify distributors (both online and on-site) on procedural support, troubleshooting, and clinical education standards.Maintain flexible availability to support urgent, distributor-notified cases, which may involve travel.Clinical Education & Therapy DevelopmentDeliver technical presentations and hands-on workshops at hospitals, clinical meetings, and distributor events.Foster and sustain robust professional relationships with interventional cardiologists and cath lab teams to encourage therapy adoption and sustained use.Assist in the organization and execution of local registries or observational studies, including logistics coordination, IRB submissions, and data collection.Engage with Key Opinion Leaders (KOLs) to support protocol development, clinical feedback, and publication initiatives.Clinical Research & Feedback CollectionSupport clinical trial activities...

Join our dynamic team as an Assistant Relationship Manager for the APAC region. In this fully remote role, you will play a pivotal part in fostering strong client relationships and delivering exceptional service. Your ability to understand client needs and provide tailored solutions will be crucial in driving satisfaction and loyalty.As a member of Xapo, you will work in a fast-paced environment that values innovation and teamwork. Your contributions will directly impact our clients and the overall success of our organization.