6,489 Svar Life Science jobs in Indonesia
Research Associate
Posted today
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Who We Are
Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation-inspiring complex change, enabling organizations to grow, building competitive advantage, and driving bottom-line impact.
To succeed, organizations must blend digital and human capabilities. Our diverse, global teams bring deep industry and functional expertise and a range of perspectives to spark change. BCG delivers solutions through leading-edge management consulting along with technology and design, corporate and digital ventures—and business purpose. We work in a uniquely collaborative model across the firm and throughout all levels of the client organization, generating results that allow our clients to thrive.
What You'll Do
As a Research Associate within BCG Vantage's Global Research Organization (GRO) team, you will form an integral part of our South East Asia GRO team. Through the delivery of secondary research, you will contribute to BCG's client work and knowledge base by supporting proposals, client cases and business or internal development initiatives.
You will clearly synthesize, package, articulate and deliver your findings in a timely and accurate manner and conduct research on commercial, multi-industry and economic topics. Excellent organizational skills are essential for successfully managing a variety and volume of research requests by accurately summarizing data and facts into appropriate and timely output i.e. email, Excel, PowerPoint, Word. Along with supporting research products (i.e. news alerts, company profiles etc.), you will also contribute to knowledge capture and documentation.
What You'll Bring
- Undergraduate Degree minimum (a preference for a degree in business, economics, engineering, sciences)
- 0-2 years relevant working experience
- Excellent English; Native Indonesian
- Have a good understanding and experience working in Financial Institution is preferred: Banking
- Fluency in macroeconomic or Industry specific databases is a plus (Oxford Economics, S&P, Orbis, IHS Market, etc)
Who You'll Work With
Additional info
BCG Vantage is a powerhouse of expertise, seamlessly embedded within Practice Areas and markets to drive extraordinary impact. It equips BCG case teams and clients with cutting-edge expertise, proprietary assets, actionable data, and transformative insights that empower our case teams and enable our clients to achieve their aspirations.
With global experts across 20 Practices, covering more than 100 topics, sectors and offers, plus four focused geographic markets, BCG Vantage delivers unparalleled depth and breadth of insight & expertise. BCG Vantage consists of three career paths, each playing a crucial role in delivering value to clients, case teams and practice teams.
- Client Focus (Embedded Expertise) Integrates into client-facing teams to deliver direct client impact through expertise, know-how, and proprietary tools and assets
- Topic Activation (Sector Expertise with Proprietary Tool & Data Solutions) Combines deep domain insights with our know-how and proprietary assets to address targeted challenges directly with clients and project teams; co-creates insights on industry trends and functional topics, proprietary data and tools, and teams to codify IP that all enables BCG to deliver excellent business value with its clients
- Research (Practice Topic and Sector-Aligned Research and Insights) Delivers actionable research and insights tailored to the client project's needs; works with qualitative and quantitative data, conducts research and provides synthesized results from sources including commercial data, public and open source, company and industry research, macro-economic, commodities and trade data.
You're Good At-
Engaging with customers
You will thrive learning in a rich, fast paced, deadline driven yet thoughtful environment that is customer focused. Working closely with more senior team members, you will engage with Internal clients daily with the aim to understand, scope and deliver accurate, timely and relevant data and information
Thinking analytically
You're an organized thinker who commits to learning research analysis including: methods, databases and tools, synthesis & packaging
Working accurately in a fast paced, deadline focused environment
You will have strong attention to detail by clarifying request objectives under direct supervision and discussing the most appropriate and timely research approach. You will do this whilst communicating directly with BCG stakeholders to evaluate and recommend the most efficient and successful research strategy per project
Working well independently and in a collaborative team environment
Working closely with fellow colleagues, you will approach all interactions with the highest level of quality and customer service. You will also guide outsourcing partners in their research analysis and do quality assurance
Seeking professional development
You will welcome the opportunity to grow and learn in an apprenticeship culture where you can quickly build and expand your research knowledge base to the next level
Communicating with confidence and ease
You will be a clear and confident communicator, able to deliver messages in a concise manner with a positive disposition and you will help build a loyal customer base for GRO
Boston Consulting Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity / expression, national origin, disability, protected veteran status, or any other characteristic protected under national, provincial, or local law, where applicable, and those with criminal histories will be considered in a manner consistent with applicable state and local laws.
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Clinical Research Associate
Posted 2 days ago
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Clinical Research Associate
Posted 4 days ago
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Clinical Research Associate
Posted 4 days ago
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Key Responsibilities:
- Conduct site initiation, routine monitoring, and close-out visits.
- Ensure compliance with study protocols, regulatory requirements, and SOPs.
- Verify the accuracy and completeness of clinical trial data.
- Manage communication between research sites, the sponsor, and regulatory bodies.
- Identify and address potential issues and risks at clinical trial sites.
- Ensure the rights, safety, and well-being of trial participants.
- Maintain accurate and up-to-date trial documentation and records.
- Provide training and support to site staff.
- Prepare monitoring visit reports and action items.
- Participate in investigator meetings and teleconferences.
- Proven experience as a Clinical Research Associate or similar role in clinical trials.
- Thorough knowledge of clinical trial phases, processes, and regulations (GCP, ICH guidelines).
- Experience with electronic data capture (EDC) systems and other clinical trial management software.
- Excellent monitoring and auditing skills.
- Strong understanding of medical terminology and research ethics.
- Exceptional communication, interpersonal, and organizational skills.
- Ability to manage multiple projects, sites, and priorities effectively in a remote setting.
- Problem-solving and decision-making capabilities.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Clinical research certifications are a plus.
Clinical Research Associate
Posted 6 days ago
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Clinical Research Associate
Posted 6 days ago
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Job Description
Clinical Research Associate
Posted 6 days ago
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Job Description
Key responsibilities include selecting, training, and managing study sites, ensuring the quality and integrity of data collected, and resolving data discrepancies. You will conduct on-site and remote monitoring visits, review source documents, and ensure that all study-related activities are conducted and documented according to the approved protocol and regulatory standards. The CRA will also serve as the primary liaison between the sponsor and the clinical sites, facilitating communication and addressing any issues that may arise. Building strong relationships with investigators, study coordinators, and site staff is essential for the successful execution of clinical trials. This position requires extensive travel to investigative sites as needed, in addition to remote monitoring responsibilities. The successful candidate will be a self-starter with excellent organizational skills, the ability to manage multiple priorities, and a proactive approach to problem-solving. A commitment to ethical research practices and patient safety is paramount. This is a significant opportunity to play a vital role in bringing life-changing therapies to patients worldwide and advancing pharmaceutical science. Your expertise will be crucial in ensuring the success of critical research projects.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical or biotechnology industry.
- In-depth knowledge of ICH guidelines, GCP, and regulatory requirements for clinical trials.
- Proven experience in site monitoring, data review, and query resolution.
- Excellent communication, interpersonal, and presentation skills.
- Ability to manage time effectively and prioritize tasks in a remote work environment.
- Willingness to travel up to 50% for site visits as required.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong critical thinking and problem-solving abilities.
- Fluency in English is essential.
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Clinical Research Associate
Posted 7 days ago
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Responsibilities include: monitoring assigned clinical trial sites to ensure protocol compliance and data accuracy; conducting site initiation visits, interim monitoring visits, and site close-out visits; verifying source documentation against case report forms (CRFs); ensuring patient safety and reporting adverse events according to regulatory requirements; educating site staff on study protocols and procedures; maintaining trial documentation and regulatory binders; resolving data queries and discrepancies in a timely manner; fostering strong relationships with investigators and site personnel; and contributing to the preparation of study reports and regulatory submissions. A Bachelor's degree in a life science or related field, significant experience as a CRA, and a deep understanding of ICH-GCP guidelines are required. Excellent written and verbal communication skills, proficiency in clinical trial management systems, and the ability to travel to sites (as needed) are essential for this hybrid role. This is an excellent opportunity to contribute to the development of life-saving medications within a dynamic and supportive pharmaceutical environment.
Clinical Research Associate
Posted 7 days ago
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Job Description
Responsibilities:
- Conduct site visits (remote and on-site) to assess protocol and regulatory compliance.
- Monitor clinical trial progress, ensuring accurate and timely data collection.
- Verify source data against case report forms (CRFs).
- Educate and support site staff on trial procedures and requirements.
- Manage communication between study sites, investigators, and the study team.
- Ensure all trial-related documentation is maintained accurately and compliantly.
- Identify and address potential issues and risks at clinical trial sites.
- Participate in investigator meetings and provide training to site personnel.
- Prepare monitoring reports and follow up on action items.
- Adhere to all company policies and procedures, as well as GCP and relevant regulatory guidelines.
This is a hybrid position, offering a blend of remote work flexibility and essential on-site engagement. You will be part of a collaborative team committed to advancing pharmaceutical research. The successful candidate will demonstrate exceptional attention to detail, strong problem-solving skills, and the ability to manage multiple sites and priorities effectively. This role requires a balance of independent work and interpersonal collaboration, contributing to our client's mission in Bandung, West Java, ID .
Clinical Research Associate
Posted 8 days ago
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- Conduct pre-study, initiation, monitoring, and close-out visits to clinical trial sites.
- Verify the accuracy, completeness, and consistency of clinical data by reviewing source documents and case report forms.
- Ensure compliance with the study protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements.
- Manage and resolve site-level issues, including deviations and data discrepancies.
- Train and support site personnel on study procedures and regulatory requirements.
- Monitor patient safety and report adverse events promptly.
- Maintain accurate and organized study documentation, including site files.
- Communicate effectively with investigators, study coordinators, and internal project teams.
- Prepare site monitoring visit reports in a timely manner.
- Contribute to the development of study protocols and other study-related documents.
- Bachelor's degree in a life science, nursing, or related field.
- Proven experience as a Clinical Research Associate or similar role in the pharmaceutical industry.
- In-depth knowledge of GCP, ICH guidelines, and local regulatory requirements.
- Experience with various therapeutic areas is highly desirable.
- Excellent attention to detail and strong organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong written and verbal communication skills.
- Ability to work independently and manage travel schedules effectively.
- Problem-solving skills and a proactive approach to site management.