Project Manager-Clinical Trials/プロジェクトマネージャー
Thermo Fisher Scientific
Tokyo, Japan
‎‎17 時間前

Job Summary

Managers and co-ordinates all technical and service aspects of a project.

This will range from initial discussions with clients, development of the project specifications, documentation aspects of setting up the project and management of all project related activities through to project / study completion.

Responsibilities :

Assessment of clinical protocol and other client supplied study specifications inconjunction with Proposals Group, FACTS Technical Group, Clinical Supplies, Operations and Procurement to help design Supply Chain solutions to meet the needs of the trial.

Provision of data and technical input to the Proposals group to help them in the creation of proposal.

Working with the client to finalize logistics requirements. This may include Project meetings at the client site or at Fisher.

Coordination and communication of all relevant activities, both internal and external to ensure that all services and products are ready for the start of the study or as required by the client.

Overall responsibility for ensuring that activities come together in a timely manner to meet the client and study requirements.

Use of appropriate project planning tools e.g. Microsoft Project to communicate milestones and critical path activities and responsibilities.

Timely provision of reports and other information to clients.

Organization and delivery of training, including cross training of other members of Fisher where appropriate.

Provide input into the writing and review of departmental SOPs.

Participation in client meetings / bid support meetings / teleconferences, where appropriate.

Conduct training at Monitor / Investigator meetings as required by client.

Import Licenses-Design PF’s with Clients

Invoicing - As requested, provides revenue data for submission to Finance.

Revenuerecognition - Monitor and record change in the scope of contracts. Arrange for additional invoicing as required. Ensure accurate and regular invoicing is completed

Client / Site Enquiry management - Receipt of study related calls issues, log calls inTrackwisesystem follow escalation procedure as appropriate.

Monitor call logging system to ensure calls are closed out in a timely manner.

Assignment of Inventory data - Requests assignment of component and receiving lot numbers to the Inventory system

Good Manufacturing Practice - Investigates and reports on internal non-conformances. Assists others in investigations to issues not relevant to assigned studies.

Accuracy - Responsible for ensuring a high degree of accuracy within the Distribution process.

Receipt of study materials - Co-ordinate receipt of finished goods deliveries from clients

19.Participation in cross-functional business process improvement activities as required.

Minimum Qualifications :

Education / Qualification

Degree holder, Degree in scientific / health care / business studies or related

Experiences

Project Management or Customer Servicein distribution / Logistics for10years or more

Clinical trials or commercial pharmaceutical industry is preferred

Ability / Skills

Understanding of logistical countries requirements

Flexible and adaptable with strong customer management skill

Able to analyze problems and define solutions

Able to work under pressure and to support others within team

Knowledge of warehousing and logistics work practice from the Pharmaceutical industry

Good written and verbal English skill

この仕事を報告する
checkmark

Thank you for reporting this job!

Your feedback will help us improve the quality of our services.

応募
自分のEメール
"続行" をクリックすると、私は neuvoo の同意を私のデータを処理し、私に電子メールのアラートを送信するには、neuvoo の プライバシーポリシー の詳細を与える。私の同意を撤回するか、いつでも退会することがあります。
続行
応募フォーム