Associate Clinical Study Excellence Scientist

Location: Bellprat

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where Health for all, Hunger for none is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us.

If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Associate Clinical Study Excellence Scientist
Purpose
The Assoc. CSES is a member of the core study team. The role will serve as a key liaison for the medical aspects of a trial within the study team. It encompasses ensuring the quality and integrity of medical study data and optimization of drug development within the trial’s framework. The Assoc. CSES supports the CSES or works independently in less complex trials.

Geographical Scope
Global

Key Responsibilities
In this role, you:

Contribute to the medical sections of the study protocol and other study documents

Provide input for the medical sections of clinical study reports and annual report documentation

Perform medical review and analysis of safety data to detect trends and address discrepancies

Prepare the safety aggregated report for cross‑functional review

Develop and maintain the Medical Review Plan (MRP)

Provide expertise for study tool setup and maintenance (eCRF, eCRF Completion Guidelines, clinical database UAT, data analysis, and visualization systems)

Support in preparing materials for use in presentations and advisory committee meetings

Support training on medical aspects of the study to internal and external stakeholders

Serve as the first point of contact on medical issues of assigned studies

Ensure GCP compliance in the medical aspects of the study

Support protocol deviations cross‑functional review, as appropriate

Review CIOMS reports and narratives in the clinical study report (CSR)

May work with the study team on study site feasibility

May participate in expert working groups, project standard teams, and contribute to global process improvement efforts

Value Added
The Assoc. CSES assists to ensure the medical integrity of trial conduct in clinical studies/projects while collaborating effectively with the study team on study deliverables. The Assoc. CSES supports high‑quality clinical trials and aims at drug approval.

Contribution Context
Work Interactions
Core Study Team

Global Clinical Lead / Clinical Development Lead/ Early Clinical Lead

Global Safety Lead

Country Lead Monitor / Clinical Research Associate

Qualifications
Minimum education and experience
MD, DO, PhD, PharmD, RN with a minimum of 1–2 years of industry experience in a pharmaceutical/biotech business and/or clinical experience

Preferred education and experience
MD degree is preferred.

Industry experience is not required but is a plus

Expertise, skills, and characteristics

Ability to acquire knowledge of different diseases and therapeutic areas

Proficient in GCP/ICH, FDA, EMA, and other relevant guidelines and regulations

Proactive, very flexible attitude

Adapts quickly to change

Able to work collaboratively across cultures and geographies

Organizational Relationship
Country Lead Monitor / Clinical Research Associate

YOUR APPLICATION
We welcome applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

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