Site Engagement Lead

**Career Category**:Medical Affairs
**Job Description**:If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

We are currently looking for a **Site Engagement Lead **based in Barcelona willing to be part of a high-performing team.

**Leadership of Operational Site Engagement**:

- Align and lead identification and strategic partnership with key sites to implement a collaborative initiative for clinical trial execution.
- Accountable for strategic long-term operational partnerships with key sites, provide local intelligence, and contribute to maintaining a consistent and coherent voice as part of Amgen’s overarching engagement strategy. Collaborate with other cross functional roles for ‘tailored’ global execution of study(ies).
- Primary site-facing, cross-study, operational decision-maker between Amgen and designated key sites for the purposes of establishing Amgen-Institutional operational working practices.
- Maintain country expertise, site knowledge to navigate with Amgen and sites with targeted and tailored communication.
- Develop, drive and monitor site operational strategies and performance across all therapeutic areas and studies, in strong collaboration with Amgen partners.
- Assimilate and report external feedback to evaluate and propose operational process efficiencies, focus and direction for site collaboration on clinical trials.
- Orchestrate relationship management and strong internal alignment with Amgen stakeholders (medical, study management, site management, and other key -stakeholders) to drive operational efficiencies.
- Strong collaboration with Regional and/or Local Trial Manager (RCTM/LTM*) to ensure clear roles and responsibilities. Communicate cross-study lessons learned and maintain consistent working relationships with sites.
- Share information and cross-study KPIs to Key Stakeholders, e.g. DOM, DFM, CTOM, Study Managers etc.

**Locally accountable for key, targeted sites execution of clinical studies**:

- Build and develop strong relationships with key sites to engage with Amgen as Choice for clinical trial participation, to effectively advance site operational engagement and better understand current site processes to enhance our clinical trial execution.
- Regular communication with key sites to connect on all trials/all stages to determine trends and opportunities and enhance site’s experience with Amgen. On-site visits as appropriate (per site and situation).
- Maintaining quick and direct access to key sites’ leadership & operation teams, point of escalation for operational, cross-study potential barriers and operational issues.
- Internal point of contact to navigate working with key sites, and to help key sites navigate working with Amgen.
- Centralize and socialize site intelligence technology, such as working practices, operational documents, to enhance clinical trial efficiencies at site.
- Participation in cross-functional task forces / process improvement groups.

**GSO quality management**:

- Actively participates in role forums including local and global functional and cross-functional initiatives.
- Participates in Functional Management Team (FMT) Meetings as required and applicable country-level project review meetings.

**Basic Qualifications**:

- Life Science Degree
- 7 years of work experience in life sciences or medically related field, including biopharmaceutical clinical research experience (clinical research obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting)
- Country clinical operations experience and/or regional study management experience

**Preferred Qualifications**:

- M.D., D.O., PhD, PharmD, Master’s Degree
- Expertise and in-depth understanding of site engagement with clinical trials, or building and/or coordinating community research networks

**Knowledge**:

- In depth understanding of drug development process, clinical trial conduct, ICH-GCP and local regulations, requirements, and guidelines
- Project and Program management including oversight of quality, study deliverables, budgets and timelines
- Various therapeutic area knowledge
- Fluency in written and spoken English
- Clinical trial management systems and reporting tools
- Utilization of Key Performance Indicators (KPIs)

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