Skip Navigation

Embrace the opportunities for personal and professional growth

Clinical Trial Opportunities at Parexel

Clinical Trial

Clinical Operations Assistant

求人ID 64007BR ロケーション ワーヴル, Wallonia 仕事内容
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

This role is based at our Belgium Head Office situated in Wavre, The office is open planned, and you will be working in an innovative and collaborative environment.

As the Clinical Operations Assistant (COA) you will provide full administrative tasks and maintain the paper and electronic Central Files for Clinical Operation, ensuring efficiency, accuracy and quality. You will perform tracking, scanning, filing, entry and return of Case Report Forms to clients for assigned projects, upload and naming of documents to the electronic document management system, EDC User Management activities and activities associated with Impact Harmony, as appropriate. You will also to support all site management team members on local billable administrative tasks and assist with QC of Central files.

Key Accountabilities:

Project Central Files & Clinical Trial Management Systems Maintenance and Updates :

-Track, scan, code, and apply naming convention and send documents to the relevant study Work In Progress (WIP) area and Central File (CF) area of PMED as per the Central File Maintenance Plan.
- Filling and Archiving paper wet-ink documents in the Central Files office location as per the Central File Maintenance Plan (CFMP)
- Photocopy, print distribute and retrieval of documents, as needed
- Maintain basic quality check procedures to ensure accurate maintenance of documents
- Tracking/maintenance of the Clinical Trial Management System (CTMS) and study specific site trackers (Client additional request only)
- Monitoring of the status of systems and processes (e.g. annual reporting obligations, Site Compliance regarding Safety Information System (SIS) etc.) to ensure compliance

Support to all local site management team members (CMS

- Organization of translations of study document (e.g. contacting translation company, requesting approval via Oracle, following up with translation company to ensure timely delivery)
- Payment/invoice processing including internal follow up with payment specialists in Finance
- Courier shipment of study document to the sites, vender and clients
- Collection of internal signatures for site documents (e.g. confidentiality agreement or clinical site agreements) within Parexel

Overall Accountabilities

- Assumes the ability to meet the requirements of a COA with a high degree of proficiency
- Effective time management in order to meet daily metrics or team objectives
- Able to work independently but seek guidance when necessary, escalating issues as required

Qualifications

Education:

- Relevant qualification or equivalent experience required
- High school diploma – ideally degree in life science or other related background - preferred


Skills:
- Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic - Document Management System (EDMS), and MS-Office products such as Excel and Word.
- Maintain a basic knowledge and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations and applicable Parexel procedures
- Good oral and written communication skills to internal and external customer
- Ability to prioritize multiple tasks and achieve project timeline
- High commitment to and performs consistently high quality work
- Good written English skills

Knowledge and Experience:

- Experience in office management in an international environment would be advisable

In return we will be able to offer you a structured career pathway and encouragement to develop within the role including awareness and understanding of the industry. You will be well supported and your hard work will be rewarded with a competitive base salary as well as a benefits package including holiday, pension scheme as well as other leading-edge benefits that you would expect with a company of this type.


Apply today to begin your Parexel journey!
あとで応募

お知らせを受け取る

パレクセルで新しいポジションの募集が出た際、お知らせいたします。

保存したポジション

保存されているポジションはありません

すべて見る

最近見たポジション

最近見たポジションはありません

すべて見る

イベント情報 (グローバル)