Clinical Research Scientist/Coordinator

Proclinical Group; Basel; Vor Ort; CHF 90.000 - 140.000; Vollzeit

Zusammenfassung

Proclinical Group in Basel seeks 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 with cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The ideal candidate has a strong background in clinical research, especially in oncology or hematology, and demonstrates leadership, problem-solving, and familiarity with

Qualifikationen

• Experience leading clinical studies and multi-site coordination.
• Strong understanding of regulatory and ICH-GCP guidelines.
• Background in oncology or hematology is highly desirable.
• Ability to manage multiple studies and strict timelines.
• Excellent communication and collaboration skills.

Aufgaben

• Lead or support 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.

Kenntnisse

Clinical trial management

Leadership

Regulatory knowledge

Study coordination

Medical input

Ausbildung

Master's degree in life sciences

PhD/MD 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.