Privacy Officer

2 months ago


Nottingham, United Kingdom Worldwide Clinical Trials Full time

**Requisition Number**
**6237**

**Employment Type***:
**Regular**

**Who we are**

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

**What the Privacy Officer does at Worldwide**

The Privacy Officer reports to the Director, Global Data Privacy.

**What you will do**
- Support key initiatives, such as global Data Privacy intelligence database and international data transfer compliance projects. Support development of privacy impact assessments.
- Support Director, Global Data Privacy in conducting privacy training for business functional areas on best privacy practices and regulatory obligations. Assist Director, Global Data Privacy in mitigating/eliminating key legal and regulatory privacy exposure globally, managing set projects, working with relevant business and support units.

**What you will bring to the role**
- High degree of personal and professional integrity and professional ethics, including understanding of conflicts of interest. Extensive experience with international business and diverse business cultures.
- Integrity, initiative, organization, perseverance, discretion, ability to assert themselves in difficult circumstances.
- A passion for data privacy.
- Ability to comfortably and effectively interface with clients, vendors, (academic) investigative sites and regulators. Flexible, adaptable and able to work under pressure.
- Commitment to continuing education and professional development.

**Your experience**
- Three years experience reviewing and negotiating contracts required, preferably in a regulated industry, with at least one year experience primarily in data privacy, preferably in a Contract Research Organization (CRO) or clinical division of pharmaceutical/biotech company. Advanced knowledge of global data protection and privacy laws and regulations, including but not limited to GDPR, required.
- Fluency in English language required.
- Experience advising on legal, compliance and operational matters in the clinical research space, including but not limited to data processing agreements, clinical trial agreements, patient informed consents, and privacy notices preferred.

**Why Worldwide**
At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.


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