Senior Associate, Aggregate Reporting Physician

• Advanced degree required: PharmD, PhD, MD, MPH, MS, or equivalent scientific discipline.
• 3–6 years of experience in pharmacovigilance, drug safety, medical writing, regulatory writing, or related pharmaceutical, consumer health, or medical device industries.
• Experience preparing safety and pharmacovigilance documents preferred.
• Familiarity with global pharmacovigilance regulations and safety reporting requirements.
• Experience working in a matrixed environment with multiple stakeholders.
• Strong understanding of: Clinical research methodologies, Epidemiology and biostatistics, Evidence-based medicine, Regulatory and scientific communication requirements, Safety and benefit-risk assessment principles
• Expertise in literature evaluation and scientific data interpretation.
• Ability to critically analyze multiple complex scientific information and identify key insights to drive product safety.
• Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) with strong document formatting, data analysis, and presentation capabilities.
• Excellent medical writing, editing, and proofreading skills.
• Exceptional grammar, attention to detail, and document quality standards.
• Strong analytical and critical thinking capabilities.
• Effective project management and organizational skills
• Exceptional Communication and Presentation Skills, with the ability to convey complex clinical and scientific information clearly and effectively to diverse audiences.
• Ability to work independently while managing multiple priorities and deadlines.

• Full performance and development process with end of year reviews
• Team events and end of year party
• Employee satisfaction survey - your feedback is important for continuous improvement
• Health Insurance

Once you have submitted your CV, you will receive an acknowledgement that we received it.

If you have the requirements we need, you will be invited for phone interview as the first step.

Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

Join our passionate team and make a meaningful impact on global healthcare!

Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel.

The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.

The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer.

We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity.

Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities.

We recognize this is our strength and celebrate it.