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Latest Jobs
196 listing(s) available.
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29 Mar 2019
General Manager / Managing Director / Country Manager (Fashion Retail is a must)
Hong Kong
Permanent PositionOur client, top-leading retail brands, with their expansion in Hong Kong as well as Asia Pacific, are looking for suitable candidates for General Manager / Managing Director / Country Manager to join their growing team.Job Description
- Report directly to CEO
- Establish goals and advise regional sales teams on how to improve performance globally
- Establish guidelines for key partnerships in all regions
- Analyze data to evaluate sales statistics and customer satisfaction
- Develop new markets and propose opportunities to increase sales with new customers and partners
- Motivate and manage sales staff in all regions including all recruitment, hiring and performance evaluations of key positions
- Lead coordination of sales activities in all regions
- Attend sales meetings with key customers who require support and a managerial relationship and/or who have special requirements
- Work with internal counterparts in Design, Production, Marketing, Retail to execute key sales initiatives
- Collect and provide quality feedback on product and the competitive situation in all markets to feedback to internal counterparts
- Work closely with the CEO to develop strategic initiatives across all markets and channels
- Provide regular updates on KPI’s along with Action Plans to reach monthly sales targets and achieve strategic goals
Expires on 26 Apr 2019Requirements
- University degree or above with less than 10 years solid experiences in retail sales management
- Less than 15 years of working experience in retail
- Good knowledge of HK / PRC / US / Europe / Asian region retail markets
- Strong leadership skills to build and manage retail teams
- Excellent interpersonal and presentation skills for all levels of business partners
- Proficiency in Chinese, English and Putonghua
- Travel is required
Interested Applicants please send your full resume (in Word format) together with present and expected salary to Ivan Lo:
Email: ivanlo@peoplesearch.jobs
**Only shortlisted candidates will be contacted for a more detailed discussion**
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29 Mar 2019
Senior Accountant
Singapore
Permanent PositionA reputable company in the manufacturing sector, is currently seeking for talents with GL and Management Reporting experiences to join their organization.Job Description
- Manage month end closing which comprises of GL, AP and AR functions.
- Review journal entries, schedules, intercompany reconciliation and cash flow forecast.
- Prepare GST submission, tax computation and financial audit schedules.
- Responsible in the preparation for balance sheet schedules, variance analysis, budgeting and forecasting.
- Ensure financial data are maintained in compliance with the company’s policies and procedures.
Expires on 28 Apr 2019Requirements
- Degree in Accountancy
- Minimum 5 years of relevant experience in accounting with audit background
- Self-starter, hands on and meticulous individual with good communication skills
- Able to work independently with high degree of commitment in meeting tight deadlines
- SAP experience will be an added advantage
If you are interested, apply today.
Office Location: North
Kindly indicate your current/last salary details and your notice periodInterested candidates kindly forward your CV to janetlee@peoplesearch.jobs (Janet Lee Hui San, Reg No: R1879219)
Feel free to forward this great opportunity to someone who would be a great fit for this role.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 -
29 Mar 2019
Research Associate
Japan
Permanent PositionSyneos - Join a game－changing global company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies we bring together more than 21,000 clinical and commercial minds to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.Job Description
Primary Function:
The position is responsible for supporting all aspects of Real World Late Phase （RWLP） Research and driving study design, project execution, and thought leadership. This position will report to directly to a Principal, VP, or SVP, Real World Evidence Consulting Manager.
Major Responsibilities:
· Late Stage Research Support
o Conduct literature reviews and other background research to support late stage research initiatives
o Contribute to project teams to drive timely ＆ expeditious execution of late stage research projects
o Contribute to proposal development and preparation of bid defense materials to assist in winning new late stage projects
o Prepare presentation materials （in PowerPoint） and assist in document development （in Word ＆ Excel） for late stage proposals, reports, manuscripts, posters, etc.
·Materials/templates will be housed within the RWLP portal and will be the primary documents to support new business opportunities
Responsible for performing activities that are in compliance with applicable Corporate and Divisional Policies, Standard Operating Procedures and Operating Guidelines and performing other duties as assigned by management.
Note: This job description describes the principal and main elements of the job. It is a guide to the nature and main duties of the job as they currently exist, but is not intended as a wholly comprehensive or permanent representation.Expires on 28 Apr 2019Posted By
Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書（英語版、日本語版でも可）を 表記のメールアドレスまでご送付いただけますとスムーズです。)Tel: 080-1118-4497
nagai.m@peoplesearch.jobsRequirements
【必須（MUST）】
Education Required:
· BA/BS or Master’s in economics, mathematics, statistics or related quantitative field.
· Relevant job experience in designing and implementing late stage studies is desirable.
Minimum Training ＆ Experience Required:
· Up to two （2） years of experience preferred.
· Strong personal communication and staff management skills and experience preferred.
· Other experience includes extensive experience with personal computers; knowledge of statistical software; fluent in written English.
· Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
·Ability to travel as necessary （approximately 5％）
Disclaimer:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
給与は前職考慮の上で決定いたします -
29 Mar 2019
Project Specialist, Real World Evidence
Japan
Permanent PositionSyneos - Join a game－changing global company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies we bring together more than 21,000 clinical and commercial minds to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.Job Description
JOB SUMMARY
The Project Specialist performs administrative and supportive activities assigned by the Project Lead to ensure the contracted services and expectations are carried out by the project team in accordance with executed contracts and the customers’ expectations.
JOB RESPONSIBILITIES
· Set－up, maintain and/or close out project files and study information （（e.g., regulatory documents, Trial Master File （TMF）, enrollment, Adverse Events （AEs）/Serious Adverse Events （SAEs）, site supplies, Institutional Review Board re－approvals, data queries） on a variety of databases and systems.
· Attends, participates, prepares and distributes meeting minutes and action items for both internal and external meetings （sponsor, trusted process, functional, investigator meetings）. Follows up with team members on action items to closure.
· Maintains timely and effective communication among team members and site staff. Keeps Project Leadership and Clinical Research Associates （CRAs） fully appraised of sites and study status. May contact site staff as needed for critical information.
· Provide administrative support to Project Leads and functional leads.
· Ensure all study documents are archived based on the appropriate guidelines and policy.
· Provide support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues.Expires on 28 Apr 2019Posted By
Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書（英語版、日本語版でも可）を 表記のメールアドレスまでご送付いただけますとスムーズです。)Tel: 080-1118-4497
nagai.m@peoplesearch.jobsRequirements
【必須（MUST）】
QUALIFICATION REQUIREMENTS
· Associates Degree （or equivalent） level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience
· Knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
· Strong organizational skills.
· Ability to manage time and work independently.
· High proficiency with full MS Office Applications.
· Strong communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
· Ability to travel if necessary preferred （approximately 5％）
· High level of competence in English language
給与：前職考慮のうえ決定します -
29 Mar 2019
CTA (Clinical Trial Assitant)
Japan
Permanent PositionICON - 世界でも5本の指に入るほどの規模と実績を誇るCRO。世界23ヶ国に拠点を持ち、約3600名の社員を抱え、その日本法人である当社は海外オフィスと協力し、海外での治験データを活用して日本での治験を簡略化させる今注目の「ブリッジング」や「グローバル試験」を実践。効率的な治験の実施に向け、戦略的に取り組む製薬メーカー様より大きな信頼を得ています。Job Description
Roles and Responsibilities
•To provide general administrative support to the Commercialization and Outcomes team
• To be familiar with ICH GCP, appropriate regulations, relevant SOP’s and internal tracking systems.
• To be familiar with the roles of the Clinical Research Associates （CRA） including site visits, if appropriate.
• To assist project teams with study specific documentation and guidelines as appropriate.
• To set up, organize and maintain clinical study documentation （e.g. Main Study Files, CRFs, etc.） including preparation for internal/external audits, final reconciliation and archival.
• To process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.
• To assist in quality control audits of clinical study documentation （e.g. Main Study Files, CRF Files, Monitoring Files, etc.）.
• To co－ordinate ordering/dispatch and tracking of trial materials （e.g. CRFs, diary cards, lab supplies, drug supplies） as appropriate.
• To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
• To copy and route incoming correspondence, internal documentation, CRFs, etc., as appropriate.
• To assist in co－ordination of Investigator payments, if applicable.
• To contact clinical sites for specific requests （e.g., enrollment updates, missing documentation, meeting arrangements, etc.）.
• To assist in the tracking and distribution of safety reports.
• To attend project team meetings and generate meeting minutes.
• To assist the Project Manager and project team with Investigator Meeting coordination, activities preparation and generate meeting minutes.
• To assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.
• To assist with the coordination of team member tracking.
• Other duties as assignedExpires on 28 Apr 2019Posted By
Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書（英語版、日本語版でも可）を 表記のメールアドレスまでご送付いただけますとスムーズです。)Tel: 080-1118-4497
nagai.m@peoplesearch.jobsRequirements
【必須（MUST）】
• Language skills required: Japanese （Fluent）
English （Reading/Writing） business level
給与は前職考慮の上で決定いたします -
29 Mar 2019
【東京】PMSモニター
Japan
Permanent Positionシミック - 1992年に日本で最初にCRO（医薬品開発支援）というビジネスを開始致しました。 近年では、医療・医薬品を取り巻く環境はめまぐるしく変貌し、国境の垣根を越えた開発競争、M＆Aや異業種からの参入など、かつてないほどに業界再編の動きが激化しています。それに伴い、製薬企業を中心とするお客様のニーズも多様化・高度化していますが、私たちはそのニーズを迅速かつ的確に捉え、お客様の期待以上のサービスを提供できるよう活動してまいります。Job Description
本事業推進部は、製造販売後調査（いわゆる使用成績調査・特定使用成績調査）の共同調査におけるPMSモニタリング及び事務局業務を担当しています。なお、製造販売後調査は、GPSP省令、GVP省令を遵守して適正かつ円滑に実施することが要求されています。
役割としては、プロジェクトを統括するプロジェクトリーダー、医療機関への対応を行うPMSモニター及び共同調査の窓口対応等を担当している事務局担当となります。
製造販売後調査（（特定）使用成績調査）に関わる以下の業務
1．施設選定（Feasibility調査）
2．医師への調査の依頼
3．契約書・覚書・IRB資料作成と契約手続き、IRB審査手続き
4．セットアップ（医師への実施要綱・調査票・EDCの説明）
5．医療機関訪問による調査票回収・再調査
6．有害事象報告
7．担当施設の進捗管理
8．調査委託費の支払い
9．終了手続きExpires on 28 Apr 2019Posted By
Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書（英語版、日本語版でも可）を 表記のメールアドレスまでご送付いただけますとスムーズです。)Tel: 080-1118-4497
nagai.m@peoplesearch.jobsRequirements
【必須（MUST）】
●2019年5月、6月に入社可能な方
●以下いずれかの経験をお持ちの方
・臨床開発に係わる業務経験1年以上、もしくはMR経験2年以上
・医師、薬剤師等の医療関係者とのコミュニケーション経験のある方
（臨床研究・治験・PMSのモニター、MR、CRC、看護師、薬剤師、臨床検査技師等）
【歓迎要件】
•TOEIC600点以上
給与は前職考慮の上で決定いたします