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Making trials a lot more fun! ~ SINCE 2003 ~
スウェーデンに本社を置くファーマ・コンサルティング・グループ。製薬企業等に対して医薬品開発を様々な面から支援しています。今回、事業の拡大に伴い「プロダクトスペシャリスト」を募集!

Do you have experience from clinical trials and would like to be a part of a fast growing IT company with the world as the market? And do you think it seems like a great idea to have a central role in an organization where clinical trials meets new technology? Then you should continue to read.

We are looking for a product specialist supporting our internal organization, our sub-contractors and our worldwide customers. The role includes performance, validation and quality check of study setups, and project management for study setups that we out-source to sub-contractors. The role also includes participation in defining user requirements and user acceptance tests for new product releases.

You will be a part of our Professional Services and Partner Support team, and work closely with our business functions Sales & Marketing, System Development and Product Management.

Role Description
Building and validation of study setups, project management, training and technical support for customers, product development, sales support

Responsibility

  • Database setup- Based on a protocol, and other study specifics like CRF templates, you will perform a study setup
  • Validation- Validation of a study setup (compared to protocol, work flow, logical checks, etc)
  • Quality Control- Performance of QC of setup
  • Documentation- Participate in the producing of system documentation and manuals
  • Viedoc Support- Supporting customers in study setups and performance of studies that have gone live
  • Training- Participate in internal training of Product specialist
  • Sales support- Assist in technical sales activities and proposals
  • Project management- Manage a team performing above study setup, validation, qc and documentation of a project

Skills and competence
What we are looking for
Since PCG Solutions is a still a young company, we are looking for a person that could help us develop our business in as wide range as possible, with new ideas and an energizing driving force. We assume that all required skills and experiences stated below might not be met, and are to be considered as a starting point for an open discussion.

Skills and experiences

  • Minimum of 5 years of relevant work experience
  • Fluent Japanese and English
  • Other languages
  • Skills in written and spoken English and local language
  • Knowledge of clinical trials
  • Knowledge of relevant clinical trials guidelines
  • Knowledge of clinical data management
  • Skills in JavaScript programming
  • Project Management

Education
Academic degree in relevant disciplines or equivalent

Location
Location is Tokyo, Japan

Travel
You will be based at the Tokyo office, but will be required to travel from time to time, mostly around Japan, but also internationally.

About you
Hopefully, you will feel the power of our product Viedoc, and work with it in a passionate way. You are a team player who likes having central role, supporting both colleagues and customers. You are a person who gets things done. You think flexibility and responsibility is something positive.

About our people strategy and values
We enjoy working in a generous environment with reliable, non-prestigious and humble colleagues who respect customers, each other and decisions by being responsive, well prepared and punctual.

Understand the customer | Be reliable | Have fun

If this resonates with your goals and career ambitions, contact us applying and sending your CV. Contact our Kai Eriksson for more information if needed: Enable JavaScript to view protected content..

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スウェーデン
ウプサラ
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フィンランド
トゥルク
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ドイツ
ミュンヘン
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日本
東京)​
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中国
上海
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Pharma Consulting Group