Clinical Trial Assistant

**We see human behind every number**

**Clinical Trial Assistant**

**Location: Issy Les Moulineaux, Paris, France (hybrid
- 2 days in the office)**

On behalf of our partner, one of the global leaders in clinical research, we are seeking an experienced, motivated, reliable and dedicated **CTAs who can demonstrate a first experience as a Clinical Trial Assistant within the pharmaceutical industry or **a CRO.**

The **Clinical Trial Assistant** assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. As a Clinical Trial Assistant you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.

**Detailed Job Duties and Responsibilities**
- Trial Master File (TMF) creation and management
- Co-ordinate entry and maintain local data into study management systems including setting up new studies
- Ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission
- Track and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations/materials
- Process, reconcile, distribute and track essential documents and submit them to local archive in compliance with SOPs
- Complete tracking documentation as applicable including but not limited to spreadsheets, study and contract tracker
- Prepare and review site communication documents
- Set-up/maintain courier accounts and organize shipments

**Education / Qualifications / Skills Requirements**
- A first stable experience as a CTA, this within the pharmaceutical industry or a CRO
- Excellent organization skills
- Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
- Strong IT skills
- Strong communication with the ability to multitask and work effectively under pressure
- Fluency in French and professional proficiency in English

**Benefits**:

- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
- Global Employee Assistance Program
- Life assurance
- Country-specific flexible benefits, including options like gym membership discounts, childcare vouchers, and more.

KCR is a clinical development solutions provider creating value for emerging biotechnology organizations.

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KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.