Cra I

il y a 7 jours

Paris, France ICON Temps plein

We are seeking **motivated, reliable, and dedicated Clinical Research Associates (CRAs)** with at least **1 year of experience** as a CRA within a **CRO**. Ideally, you should have experience in **Oncology** and **Onco-Hematology**, although other therapeutic areas will also be considered, especially if gained in **Phase I - III commercial trials**.

As a **Clinical Research Associate**, you will be dedicated to one of our **global pharmaceutical clients**, where we share a culture of **innovation**, **flexibility**, and a common vision to bring life-saving treatments to market. You will set the standard for excellence and enjoy a challenging and rewarding career within our exclusive programs.

We are currently looking for a **CRA based in the Paris area**, who is willing to travel to the **Sponsor's office** for **study meetings** and **team meetings** (around **once a month**).

**Key Responsibilities**:

- Take **full ownership** of investigator sites for assigned studies, managing the site from start to close-out.
- Plan and conduct **site visits** (feasibility, site selection, interim, and close-out) in accordance with the clinical monitoring plan.
- Build strong relationships with **investigator site staff** to ensure key clinical metrics are met.
- Prepare for and attend **investigator meetings**, coordinate the timely shipment and proper storage of clinical supplies, and follow-up on drug safety issues.
- Ensure the **integrity of clinical data**, maintaining site tracking records and adhering to relevant guidelines.

**What You Need**:

- ** At least 1 year of CRA experience** within a **CRO**, ideally in **Oncology and Onco-Hematology** studies.
- ** Excellent organizational skills**, with the ability to manage multiple priorities effectively.
- Ability to work well in a **dynamic environment** and respond to the changing needs of the business.
- ** Strong IT skills** and the ability to multitask and work under pressure.
- ** Strong communication skills** and the ability to work effectively with site staff and stakeholders.
- ** Fluency in French** and **professional proficiency in English**.
- Willingness to travel to the **Sponsor's office** in **Paris** for study and team meetings (approximately once per month).

**Why Join ICON?**:
At ICON, our **Clinical Operations team** is renowned for its excellence. You will receive the support and training you need to grow personally and professionally in an environment that values your contributions. Our team works closely together to solve challenges, build strong relationships, and drive success. As a CRA, you will play a crucial role in our clients' drug development processes as part of a global study team.

LI-KD1

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