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Latest Jobs
86 listing(s) available.
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18 Jul 2019
General Compliance AVP/VP
Singapore
Permanent PositionA foreign bank looking to expand its presence in Singapore is looking for an experienced Compliance professional. This will be a great opportunity for you to establish your career in a General Compliance function, while contributing to the bank’s Anti Money Laundering/Countering the Financing of Terrorism (AML/CFT) and Regulatory Compliance framework and test plan. You will work closely with stakeholders across the bank, and gain visibility with senior management. In return, you will receive a generous remuneration of up to $120,000 per annum.Job Description
- Enhance the existing Compliance and AML testing framework, and conduct testing
- Document, draft and present findings to relevant stakeholders and senior management
- Assist to oversee KYC, transaction monitoring and sanction clearance and checks
Expires on 17 Aug 2019Requirements
- At least 7-10 years of experience with relevant work experience focusing on controls/ QA/AML/Compliance testing/Financial Crime Compliance
- Knowledge of local regulatory framework and practices including those pertaining to KYC/AML/CFT regulations
- Relevant experience with SFA/FAA would be a bonus
- Meticulous, hands-on, independent and motivated to accomplish tasks on time
Interested candidates kindly forward your CV to agneschan@pplesearch.com (Agnes Chan Suan Tsing, Reg No: R1768753).
All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.
PeopleSearch Pte Ltd
EA License No: 16S8057 -
18 Jul 2019
Biostatistician
Taiwan
Permanent PositionThe company is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. We offer a broad range of solutions that harness advances in healthcare information, technology, analytic.Job Description
- Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis.
- Assist with protocol development, sample size calculation, and protocol and case report form (CRF) review.
- Advise data management staff on database design, validation checks and critical data.
- Assist project lead in fulfilling project responsibilities.
- Under supervision, manage project budget and resource requirements. Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies.
- Provide training and guidance to lower level and new staff. All responsibilities are essential job functions unless noted as nonessential (N).
- Excellent written and oral communication skills including grammatical/technical writing skills
- Familiarity with basic statistical methods that apply to Phase I-IV clinical trials
- Strong aptitude for, and working knowledge of SAS computing package
- Ability to effectively manage multiple tasks and projects
- Ability to accept direction of lead team members
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
Expires on 17 Aug 2019Requirements
- Master's degree or educational equivalent in biostatistics or related field; Bachelor's degree or educational equivalent in biostatistics or related field and 1 year relevant experience; or equivalent combination of education, training and experience
- PHYSICAL REQUIREMENTS
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17 Jul 2019
Data Manager
Taiwan
Permanent PositionThe company is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. We offer a broad range of solutions that harness advances in healthcare information, technology, analytic.Job Description
- Manage and co-ordinate efforts of cross-functional project teams. Ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures. Implement continuous improvement activities for assigned projects.
- Develop study management plans, together with team assignments and accountabilities and oversight of database maintenance.
- Serve as primary project contact with Sponsor to ensure communication is maintained and continuously improved and reporting schedules are adhered to.
- Report on team performance against contract, customer expectations, and project baselines to management.
- Lead problem solving and resolution efforts to include management of risk, contingencies and issues. Develop proactive contingency plans to mitigate clinical risk.
- Identify quality issues within the study through regular review of site communications, monitoring visit reports, data flow information and quality assurance audit findings to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
- Provide input for the development of proposals for new work and project budgets.
- Provide input to line managers of their project team members’ performance relative to project tasks. Recommend team members’ further professional development. Support staff development. Mentor less experienced CPMs.
- Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team.
- Prepare and present project information at internal and external meetings.
- Participate in proposal development. May lead bid defense presentations in partnership with Business Development and Senior Clinical Project Management staff.
- Define project workloads and assignments. Develop and oversee maintenance of internal databases and project plans.
Expires on 17 Aug 2019Requirements
- Person with at least one year of data management work experience
- We care about communication with customer and the company
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17 Jul 2019
Business Consultant
Taiwan
Permanent PositionOur client markets a portfolio of leading brands and best-in-class products primarily focused on four key therapeutic areas including medical aesthetics, eye care, central nervous system and gastroenterology.Job Description
Perform needs analysis – Work with the targeted account to identify their needs and accomplished through one on one meeting with the account discussing their goals and identifying the key elements that will enhance their success.
Develop an Action Plan – Develop a plan of action to meet account needs.
Implement the Action Plan – Lead all activities of the action plan to ensure each step is implemented effectively.
Maintain and develop relationships with accounts – Responsible for maintaining the relationship with the account post completion of the action plan.
Provide support & direction to Allergan Medical management – The BC will maintain a high level of market knowledge and educate the sales team on trends and opportunities within the evolving aesthetic market. This knowledge is typically supported by dedicated reading of medical journals and marketing information.
Expires on 16 Aug 2019Requirements
Education and Experience
- University degree in business/biochemical related with MBA preferable
- At least 2 years of experience in business development
- Proven experience in management/strategy consulting
- Significant relevant sales or marketing experience
- Strong management experience including budget and personnel
Essential Skills, Experience, and Competencies (includes Licenses, Credentials)
- Consulting Approach
- Project Management
- Business Management & Development
- Operational Business Optimization
- Marketing – preferably Customer Experience
- Leverage of Financial knowledge
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17 Jul 2019
Logistics Operation Coordinator
Taiwan
Permanent Position規劃與執行物流相關設備之維護點檢作業，並正確及效率兼具的方式完成設備維護與升級確保所有物流設備效率運作Job Description
- 完成作業設備汰舊換新之相關規劃，以利相關業務得以順利執行。
- 設備維護訓練之規劃及執行,以利物流服務供應商之主管及其他各組人員可自行排除異常維持作業效率。
Expires on 31 Jul 2019Requirements
- 3-5年以上物流作業或設備維護經驗
- 具專案規畫+問題分析解決能力佳
- 國、台語流利，具英文能力佳
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17 Jul 2019
Sr. CRA/ Lead CRA
Taiwan
Permanent PositionOur client is focused on the development of innovative new therapies to improve the world’s health. They do this by providing a suite of groundbreaking biopharmaceutical development services that help customers across the globe transform scientific discoveries into new treatments for patients. From clinical trial design to regulatory and consulting services to commercial and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.Job Description
- Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
- Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
- Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider associations
- Identify operational efficiencies and process improvements
- Develop country level informed consent forms
- Collaborate with RWLP Regulatory team to ensure updated regulatory information is applied and shared
- Participate in bid defense meetings
- Per the Clinical Monitoring/Site Management Plan
- Verifies required clinical data entered in the case report form is accurate and complete via review of site source documents and medical records
- Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines
- Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture
- Verifies site compliance with electronic data capture requirements
- May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.
- Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.
- Understands project scope, budgets, and timelines for own and others’ activities in the clinical team; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets.
- May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.
- Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.
- Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
- May provide training or mentorship to more junior level CRAs. May perform training and sign off visits for junior CRA staff, as assigned.
- May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead, or operational line manager.
- For Real World Late Phase (RWLP), the Sr. CRA I will use the business card title of Sr. Site Management Associate I. Additional responsibilities include:
- Site support throughout the study lifecycle from site identification through close out
- Knowledge of local requirements for real world late phase study designs
- Chart abstraction activities and data collection
- As required, collaborate and build relationships with Sponsor and other affiliates, medical science liaisons and local country staff
- Identify and communicate out of scope activities to Lead CRA/Project Manager
Expires on 07 Aug 2019Requirements
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
- Must demonstrate good computer skills and be able to embrace new technologies
- Fluent in English
- Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected.
- Ability to manage required travel of up to 75% on a regular basis