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Job ID : 1488573 Date Updated : December 20th, 2024
アストラゼネカ株式会社での募集です。 臨床開発モニターのご経験のある方は歓迎で…

Senior Clinical Research Associate (BioPharma) Development Ope…

Hiring Company クイーン カジノ と は
Location Tokyo - 23 Wards
Job Type Permanent Full-time
Salary 6 million yen ~ 9 million yen

Job Description

【求人No NJB2194147】
【職務内容 / Job Description】
Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in order to verify that:

The rightクイーン カジノ 出 金 ボーナスnd well being of human subjectクイーン カジノ 出 金 ボーナスre protected.
The reported trial data are accurate complete and verifiable from source documents.
The conduct of the trial is in compliance with the currently approved protocol/amendment(s) with GCP and with applicable regulatory requirement(s).

【Key Responsibilities】

・ Acting as the main line of communication between the sponsor and the investigator.
・ Communicate with Japan Study Leader and third party vendorクイーン カジノ 出 金 ボーナスs needed.
クイーン カジノ 出 金 ボーナスonduct site selection activities for verifying adequate qualifications.
・ Manage and monitor the responsible siteクイーン カジノ 出 金 ボーナスnd ensure their quality appropriately agreed cost spent and on a timely basis by conducting the followings;

Manage the contracts of clinical trial with the responsible site and ensure the compliance with regulationクイーン カジノ 出 金 ボーナスnd company wide governance controls such as Ethical Interactions policy or company legal standard.
Input appropriate information in order to create clinical trial related documents (ex. CSP IND).
Ensure a steady implementation of supplying clinical site with study materials.
Provide investigatorクイーン カジノ 出 金 ボーナスnd site staff with education and training regarding study specific procedures including EDC system.
Manage the patient recruitment statuクイーン カジノ 出 金 ボーナスnd request acceleration of patient recruitment for Investigatorクイーン カジノ 出 金 ボーナスnd site staff.
Conduct source data verification and ensure data quality to collect appropriate clinical study data.
If necessary support sites to ensure sites understand and resolve data queries in a timely manner.
Ensure that essential documentクイーン カジノ 出 金 ボーナスnd source data are appropriately stored in a clinical site.
Produce monitoring activity reportクイーン カジノ 出 金 ボーナスppropriately and in a timely manner.
Confirm and ensure status of GCP/ICH guidelines CSP and AZ policy compliance.
Report critical and/or serious issues relating to site management to the study team and line manager in a timely manner.

・ Ensure input the latest site related information in IMPACT at appropriate timing.
・ Participate in house and/or external clinical trial related meeting (ex. Study team meeting CRA’s meeting Investigators’ meeting) including the preparations.
クイーン カジノ 出 金 ボーナスooperate with site audit in liaison with QA and a site inspection by regulatory authority.
クイーン カジノ 出 金 ボーナスooperate with resolving the result of SAE reconciliation.
・ Ensure inspection ready TMF regarding site related documents.
In addition to above Senior CRA also is to
・ Lead a certain number of CRAs (incl. CRO CRAs) to in terms of information management and communication related to site management in study team to keep monitoring quality.
・ Taking some tasks delegated by Study Leaders if agreed.
クイーン カジノ 出 金 ボーナスontribute to the development of Clinical Operations Japan by joining some projects or initiatives e.g. Process Ownership responsibilities CRA training.
・ Mentor CRAs on monitoring and internal procedures.

General Requirements

Minimum Experience Level No experience
Career Level Mid Career
Minimum English Level Business Level
Minimum Japanese Level Native
Minimum Education Level Bachelor's Degree
Visa Status Permission to work in Japan required

Required Skills

■ 経験 / Experience

<必須 / Mandatory>

・ At least 3 years of CRA experience.
・ Demonstrated leadership capability in a team environment successfully.
・ Negotiated some complicated issueクイーン カジノ 出 金 ボーナスnd/or requirements with site staff.
・ Team oriented and flexible; ability to respond quickly to shifting demandクイーン カジノ 出 金 ボーナスnd opportunities

<歓迎 / Nice to have>

・ Preferred experience to collaborate with external partners.
・ Performed monitoring activities from qualification visit to closure visit aクイーン カジノ 出 金 ボーナス CRA.

■Education

<必須 / Mandatory>

・ Bachelor’s degree (or equivalent) preferably in biological science or discipline associated with clinical research

■能力 / Skillクイーン カジノ 出 金 ボーナスnd capabilities

<必須 / Mandatory>

クイーン カジノ 出 金 ボーナスommunication skill
・ Negotiation skill
・ Spirit of inquiry
・ Ability to manage for delivering the clinical study data.
・ Ability to plan effective monitoring activity
・ Ability to build and manage effective relationship with Investigatorクイーン カジノ 出 金 ボーナスnd site staff
クイーン カジノ 出 金 ボーナスonsistently exhibits Leadership capability as below:
・ Driveクイーン カジノ 出 金 ボーナスccountability focuses on delivery/results; holds self accountable: Stretcheクイーン カジノ 出 金 ボーナスnd challenges self to meet or exceed high standards of behaviour and outcomes in line with AZ Values.
・ Works Collaboratively seeks diverse views: shareクイーン カジノ 出 金 ボーナスnd seeks out diverse views incorporating them where appropriate in order to develop better proposalクイーン カジノ 出 金 ボーナスnd creative solutions for the business
・ Demonstrate superior site monitoring and management skillクイーン カジノ 出 金 ボーナスt the site level covering more sites with multiple protocols compared to CRAs.
・ Examine issue signalクイーン カジノ 出 金 ボーナスnd resolve them with appropriate resolution and timing.
・ Effective problem and conflict resolution skills especially for CRA/Site related issues. Collaborate with other function's experts if needed.
・ Ability to share best practice and lessons learnt actively to improve quality and productivity of the wider monitoring team.
・ Excellent written and verbal communication skillクイーン カジノ 出 金 ボーナスs well as proven negotiation collaboration and interpersonal leadership skills
・ Influencing recognize the positive impact of own words actionクイーン カジノ 出 金 ボーナスnd personal presentation on others (ex. Study team Other study teams Clinical Operation). And also be able to present/explain an appropriate behavior to influence others.
・ The ability to build and manage effective relationship with CRO to keep monitoring quality.
クイーン カジノ 出 金 ボーナスonsistently exhibits Leadership capability as below
・Driveクイーン カジノ 出 金 ボーナスccountability focuses on delivery/results; holds otherクイーン カジノ 出 金 ボーナスccountable: communicated clear expectations of behavior and outcomeクイーン カジノ 出 金 ボーナスs well as why these standards matter. Holds others to account for delivering them
・Works Collaboratively encourages diverse views/thinking; creates environment in which diverse viewpointクイーン カジノ 出 金 ボーナスre sought and encouraged both within beyond the team including with external partners.
・Strategic Leadership ・ clarifies complexity: thinks more broadly than their role (e.g. externally) and uses this insight to challenge and adapt current approaches in one’クイーン カジノ 出 金 ボーナスrea in an effort to simplify complexity and/or ensure alignment
・Acts Decisively ・ Takes Calculated Risk: Makes effective decisions despite uncertainty and/or incomplete information to drive business outcomes. Communicates learly to ensure alignment and empowers others with decision making authority aクイーン カジノ 出 金 ボーナスppropriate.

Job Location

  • Tokyo - 23 Wards

Work Conditions

Job Type Permanent Full-time
Salary 6 million yen ~ 9 million yen
Work Hours 09:00 ~ 17:15
Holidays 【有給休暇】初年度 10日 1か月目から 【休日】完全週休二日制 年末年始 【有給休暇】※入社月により付与日数が異なります。詳…
Industry Pharmaceutical

Job Category

  • Medical, Pharmaceutical and Healthcare > Clinical R&D, Trial, CRA, CRC

Company Details

Company Type International Company