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Medical Director - Phase II-IV & RWE Studies

Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Advanced degree in a relevant scientific field., Extensive experience in clinical research., In-depth knowledge of oncology and rare diseases., Proven ability to lead complex projects..

Key responsabilities:

  • Lead scientific strategy for clinical trials and RWE studies.
  • Develop innovative study designs and proposals.

UBC logo
UBC Pharmaceuticals Large https://www.ubc.com/
1001 - 5000 Employees
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Job description

As leaders in the pharmaceutical support industry, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation. 
 

Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values of Respect, Accountability, Innovation, Quality, Integrity, and Collaboration. We believe in an inclusive workplace that fosters creativity.

If you are seeking a career that will challenge, inspire, and reward you, join us at UBC! 

Brief Description:  

We are seeking a highly motivated and experienced Scientific Leader to join our team. In this critical role, you will provide expert scientific guidance and strategic leadership to our pharmaceutical and biotech clients. Your primary responsibility will be to lead the development of innovative study designs and proposals for Phase II-IV and Real-World Evidence (RWE) studies.

 Key Responsibilities:

• Scientific Strategy: 

  • Lead the development and execution of strategic scientific plans for complex clinical trials and RWE studies.
  • Collaborate with cross-functional teams to align on scientific objectives and study design.
  • Leverage clinical and therapeutic area expertise to provide consultative support to clients.
  • Provide scientific expertise to inform study design, protocol development, and data analysis plans.

• Study Design and Proposal Development: 

  • Lead the development of innovative and scientifically rigorous study designs, including decentralized, adaptive trial designs and RWE studies.
  • Prepare compelling proposals that effectively communicate scientific value and address client needs.

• Client Engagement: 

  • Build strong relationships with clients and serve as a trusted advisor.
  • Proactively identify client needs and provide strategic solutions.
  • Present scientific concepts and study results to clients in a clear and concise manner.
  • Support business development initiatives through conference attendance, podium presence, and collaboration with the sales team.

• Team Leadership: 

  • Mentor and develop junior team members, fostering a culture of scientific excellence.
  • Collaborate effectively with cross-functional teams, including biostatistics, data management, epidemiology, project management, and clinical operations.

• Regulatory Compliance: 

  • Ensure adherence to regulatory guidelines (e.g., ICH-GCP, FDA, EMA) and industry best practices.
  • Subject matter expertise on regulatory trends and emerging scientific methodologies. 

Qualifications:

• Advanced degree (Ph.D., PharmD, MD) in a relevant scientific field (e.g., medicine, pharmacy, epidemiology, biostatistics).

• Extensive experience in clinical research, with a strong focus on Phase II-IV and RWE studies.

• In-depth knowledge of oncology and rare disease therapeutic areas.

• In-depth knowledge of clinical trial methodologies, regulatory requirements, and data analysis techniques.

• Proven ability to lead complex projects and deliver high-quality results.

• Excellent communication and presentation skills, both written and verbal.

• Strong leadership and interpersonal skills to build and maintain effective relationships with clients and team members.

• Ability to work independently and as part of a team.
 

Benefits:

At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally. 

Here are some of the exciting perks UBC offers:

  • Remote opportunities
  • Competitive salaries
  • Growth opportunities for promotion
  • 401K with company match*
  • Tuition reimbursement
  • Flexible work environment
  • Discretionary PTO (Paid Time Off)
  • Paid Holidays
  • Employee assistance programs 
  • Medical, Dental, and vision coverage
  • HSA/FSA
  • Telemedicine (Virtual doctor appointments)
  • Wellness program
  • Adoption assistance
  • Short term disability
  • Long term disability
  • Life insurance
  • Discount programs

 

UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients.

#LI-Remote

#LI-RL1

 

 

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Mentorship
  • Social Skills
  • Teamwork
  • Presentations
  • Communication

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