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Clinical trials specialist

Curitiba
beBeeDermatology
Anunciada dia 19 dezembro
Descrição

Job Title: Medical Science Liaison


Job Description:

As a Medical Science Liaison, you will serve as a key scientific resource for stakeholders, facilitating clinical trial activities and generating insights to inform strategy and improve patient outcomes.


Clinical Trial Support:

* Collaborate with clinical trial teams to support trial enrollment efforts, including identifying suitable patients and optimizing recruitment strategies.
* Engage with clinical trial sites and investigators to ensure smooth trial operations and alignment with study objectives.
* Provide education and training to clinical sites on study protocols and therapeutic areas.


Insight Generation and Framework Creation:

* Gather and synthesize insights from healthcare professionals (HCPs), patients, and other stakeholders to identify referral patterns, challenges, and opportunities for trial enrollment.
* Develop frameworks to streamline patient identification and referral pathways.


Stakeholder Engagement:

* Build and maintain relationships with HCPs, clinical trial investigators, and other key opinion leaders (KOLs) in dermatology.
* Act as liaison between clinical sites, investigators, and internal teams to ensure effective communication and support.


Cross-Border Collaboration:

* Work across national borders to address global clinical trial needs and ensure compliance with international regulations and cultural nuances.
* Collaborate with global teams to align on strategies and share best practices.


Qualifications and Experience:

* Minimum 3 years of experience as Medical Science Liaison or similar role.
* Strong background in dermatology or rheumatology, with experience engaging with dermatologist-focused clinical trial sites and investigators.
* Proven track record of supporting clinical trial enrollment, patient identification, and site engagement.
* Experience generating insights and developing frameworks to address complex challenges in clinical trial operations.
* Demonstrated ability to identify patient referral patterns and address barriers to patient participation.
* Willingness to travel extensively, including international travel.
* Experience working in cross-border settings and collaborating with global teams.
* Exceptional interpersonal and communication skills, with ability to build relationships with diverse stakeholders.
* Strong organizational and time-management skills, with ability to work independently.

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