Skip to main content

Clinical Trial Coordinator - Netherlands

Location Ede, オランダ Job Id R-01310007 Job Type フルタイム Category 臨床開発 Remote ハイブリッド
検索結果に戻る
前のジョブ 次の仕事
JOB DESCRIPTION

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Clinical Trial Coordinator - Ede, Netherlands (Hybrid)

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our clinical department defines, develops and delivers clinical programs, ensuring the highest-quality review of data and effective interaction with study sites.

As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract. Additional key responsibilities include:

  • Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools

  • Reviews regulatory documents for proper content

  • Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified

  • Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments

  • Assists with the identification of potential investigators and development/distribution of initial protocol packets

  • Crafts meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
     

Education and Experience:

  • University degree, or equivalent in education, training and experience

  • Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout

  • Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency

  • Experience of manage multiple projects with differing priorities at one given time

  • Outstanding communication, teamwork, organizational and time management skills

  • Good English and Dutch language skills

Close the popup
img1
当社は、応募にあたり何らかのサポートが必要な候補者の方は詳細をご覧ください
詳細を見る

類似した求人の通知を受け取る

サインアップし、類似した求人アラートをEメールで受け取る

成功！類似した求人に登録しました 失敗！この求人にはすでに登録済みです 失敗！類似した求人に登録できませんでした

類似の仕事

おすすめが見つかりません

How would you rate your experience popup
キャリアサイトのクッキー設定
個人情報