Site Care Partner I - Israel - FSP

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at Site Care Partner (SCP), home-based, in Israel.

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.

We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.

As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.

Our Site Care Partners work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

The most significant aspect of this position is that

-          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

From you we expect

• A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology

• In general, candidates for this job would hold the following levels of education/experience: 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)

We will offer you

• 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.

Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related Parexel FSP departments.

For an immediate interview, please contact marta.kuniewicz@parexel.com