[Hiring] Site Care Partner I @Parexel

Role Description

In this role you will be the main Client point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator site.

• The Site Care Partner I (SCP I) is the “face of the client” and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and client’s reputation is upheld throughout study lifecycle.
• The SCP I is the main client point of contact for investigative sites; accountable for site start up activities through activation; accountable for building and retaining investigator site relationships and providing support from site recommendation through the lifecycle of studies; accountable for site level recruitment and operational success, and accountable for safeguarding the quality and patient safety at the investigator site.
• The SCP I contributes to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies and client pipeline opportunities under supervision.

Qualifications

• A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology.
• BS/BSc/MS/MSc or equivalent + 5 years of clinical research experience and/or quality management experience.
• Skills in more than one language are an advantage in this role; English is required.
• Site Management/Monitoring (CRA) experience needed (at least 8 years).
• Experience in report review.
• Oncology experience.
• Solid knowledge of clinical development processes with strong emphasis on monitoring.
• Demonstrated ability to oversee a 3rd party and/or demonstrated ability in Quality Assurance (preferred).
• Project management experience preferred in the clinical development area.
• Ability to lead, troubleshoot and influence for delivery.
• Experience implementing centrally designed and developed initiatives on a local basis.
• Demonstrated knowledge of quality and regulatory requirements for applicable countries.
• Demonstrated knowledge of site intelligence at country/cluster level in support of site recommendation.
• Demonstrated knowledge of clinical trial methodology and the drug development process, related to monitoring clinical trials, GCP, Food and Drug Administration (FDA), or country-specific regulatory environment.
• Demonstrated experience in site activation and startup.
• Demonstrated networking and relationship building skills.
• Demonstrated ability to manage projects and cross-functional processes.
• Availability to travel regularly within country and region is required (3 – 5 visits per month).

Benefits

• Premium salary.
• Attractive benefits.
• Car or company car.
• Medical care plan: Health, Dental & Vision.
• Life Assurance.
• Excellent work environment.
• Culture of teamwork and collaboration.
• People who motivate and face challenges together.
• Innovative technology.
• Excellent training.