Clinical Research Scientist/Coordinator

Proclinical Staffing; Basel; Vor Ort; CHF 120.000 - 150.000; Vollzeit

Zusammenfassung

Proclinical is seeking a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, focusing on low-complexity trials. You will collaborate across cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The role requires a strong background in clinical research, particularly in oncology or hematology, with excellent leadership and problem-solving skills.

Qualifikationen

• Degree in life sciences or healthcare; advanced degree preferred.
• Experience in clinical trials; early development; multi-study management.
• Strong knowledge of ICH-GCP and regulatory/clinical finance principles.

Aufgaben

• Lead or support development of clinical protocols and amendments with Medical Lead.
• Provide medical and scientific input for study processes and regulatory documents.
• Contribute to feasibility assessments and operational execution plans.
• Collaborate to select high-performing sites to meet recruitment goals.
• Lead or support global cross-functional Clinical Trial Teams (CTTs).
• Review trial data for safety trends and data interpretation.
• Coordinate dose escalation meetings and real-time data availability.
• Manage risk mitigation and implementation strategies at trial level.
• Forecast and manage study budgets with stakeholders.
• Set vendor strategies and timelines for studies.
• Implement best practices for trial management and share lessons learned.
• Represent the group in cross-functional initiatives as SME.

Kenntnisse

Clinical research

Project management

Leadership

Communication

English proficiency

Ausbildung

Life sciences degree

Advanced degree preferred

Jobbeschreibung

Ready to be the heartbeat of clinical research? Join our client on this research scientist position and assist in turning innovative science into life-changing care!

Proclinical is seeking a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, primarily focusing on low-complexity trials. This role involves close collaboration with cross-functional teams to ensure study deliverables are met while maintaining high scientific and operational standards. The ideal candidate will have a strong background in clinical research, particularly in oncology or hematology, and demonstrate excellent leadership and problem-solving skills.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Lead or support the development of clinical protocols, amendments, and related study documents in collaboration with the Medical Lead and other teams.
• Provide medical and scientific input for study-related processes and regulatory documents.
• Contribute to study concept feasibility assessments and operational execution plans.
• Collaborate with cross-functional teams to identify and select high-performing sites to meet recruitment goals.
• Lead or support global cross-functional Clinical Trial Teams (CTTs) to ensure timely delivery of trial objectives.
• Conduct ongoing medical-scientific reviews of clinical trial data, including safety trend analysis, signal detection, and data interpretation.
• Prepare and lead dose escalation meetings and coordinate real-time availability of quality clinical trial data.
• Proactively manage risk mitigation and implementation strategies at the trial level.
• Forecast and manage study budgets in collaboration with relevant stakeholders.
• Set vendor strategies and timelines for assigned studies.
• Implement best practices and standards for trial management, sharing lessons learned across teams.
• Represent the group in cross-functional initiatives and act as a Subject Matter Expert when required.

Key Skills and Requirements:

• Degree in life sciences or healthcare (advanced degree preferred, e.g., PhD, MD, PharmD, or Master's).
• Strong understanding of clinical trial methodology, particularly in early clinical development.
• Knowledge of oncology/hematology is highly desirable.
• Experience in clinical trials or development, with a proven ability to manage multiple studies simultaneously.
• Proficiency in operational project management, including planning, prioritization, and problem-solving.
• Strong interpersonal and leadership skills to foster collaboration and inspire teams.
• High learning agility and adaptability to dynamic environments.
• Familiarity with ICH-GCP guidelines, external regulations, and clinical finance principles.
• Excellent communication skills, both written and verbal, in English.
• Commitment to diversity, inclusion, and ethical practices.

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