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.

Parexel FSP are currently recruiting for an Clinical Trial Liaison, with in depth oncology experience to join one of our growing sponsors in Germany. In this role you’ll be a vital part of the wider MSL team, your oncology experience is going to be key as the sponsors current team MSL’s do not cover oncology indications.

You’ll be identifying and building relationships with KOLs, PIs, Sub I’s and healthcare providers across the Oncology therapeutic space,

 including artificial intelligence and big data, to support trial scenario decision making.

Some specifics about this advertised role

• 100% homebased position
• Up to 60% travel
• Lead and drive site and patient engagement initiatives to improve operational excellence and performance in the clinical trial program. Also, to enhance the patient experience in trials, to improve diversity and inclusivity of patients
• Works with key stakeholders across functions to create and meet clinical operations objectives and work plans with emphasis on site and patient engagement, recruitment timelines and deliverables, and delegates assignments as appropriate.
• Lead site and patient activities cross functionally across the portfolio to achieve the group’s goals and objectives, resolving a wide range of issues in creative ways.
• Identify and communicate key clinical and research issues and insights from clinical research sites and healthcare providers to clinical study teams.
• Participate in clinical study education for healthcare professionals (HCPs) in communities around clinical trial sites. Support sites through on-site presentations at healthcare institutions in local healthcare institutions and surrounding communities.
• Provide scientific support for additional activities such as site and patient study specific material development.
• Acquires a broad understanding of local and national protocols and standards of clinical practice and trends in disease management in the US.   
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider settings in both group and one-on-one situations.
• Communicates emerging data and the clinical experience with our products through scientific exchange and peer-to-peer interactions discussing benefits and risks in an objective manner.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

What we are looking for in the this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this advertised role.

• Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 3 years of experience in oncology medicine is required, or  License (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and a minimum of 5 years’ experience in oncology medicine is required.
• A minimum of 2 years of experience as a MSL or comparable industry or clinical role is required.
• Experience in solid tumors/targeted therapies and a strong track record of success is strongly preferred.
• This is a field position, and applicants must be willing to travel ~60% of time.
• Knowledge of geography, healthcare environment and external experts in academia and medical community. 
• ​Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest. 
• ​Understanding of regulatory requirements for field-based personnel. 

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