Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.
As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
- Full Time
- Level: Mid
- Travel: Yes
- Glassdoor Reviews and Company Rating
Success Profile
Check out the top traits we’re looking for and see if you have the right mix.
- Innovative
- Problem-Solver
- Communicator
- Tech-Savvy
- Confident
- Independent
Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Compensation
Competitive salaries and bonus structure based on individual metrics.
Responsibilities
【業務内容】
臨床開発業務に関る、以下の業務をご担当頂きます。
・病院関連請求書処理
・クライアントへの請求書とりまとめ及び発送
・文書移管業務（専用システムへの文書アップロード）
・安全性情報の発送
・購買申請代行 & ベンダー関連請求書処理 （印刷・翻訳・リース）
・資材手配 （文具、リース物品、施設貸与品、印刷など） とりまとめ & 在庫管理 （購買申請対応含む）
・郵便物、社内便仕訳
・備品発注
・捺印申請のとりまとめ
・その他、必要に応じて臨床開発部員のサポート
【求める知識・経験】
・事務経験
・Excel、Word、Outlook等の基本的なOAスキル
・正確にスピード感をもって業務を行う能力
・コミュニケーション能力
・英語を使用する業務に抵抗のない方
・外資系企業での勤務経験があれば尚可
・製薬企業、CROにおいてモニターサポート経験者歓迎
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