Senior Clinical Scientist (UK, Spain, CH)

at  Global Antibiotic RD Partnership GARDP

The GARDP Clinical Scientist will provide medical and scientific study and project support primarily for clinical studies (phase I to IV) in a clinical project but also for enabling scientific workstreams at the cross project and portfolio level. She/he will work in collaboration and with oversight from the lead physician at the study and the clinical project level to develop clinical science strategies in support of the clinial development plan. Priority activities for the clinical scientist will include:

• Study and protocol design, implementation strategy, and training,
• Clinical data review and interpretation
• Safety review and coordination with drug safety
• Clinical study implementation support and oversight to ensure scientific quality, data integrity and patient safety and alignment with GARDP procedures.
• Preparation and/or review of regulatory documents, study reports and scientific publications.

The Clinical Scientist may be also lead implementation of drug/treatment project level identified by the Project Lead and/or Medical Director/ Medical Lead.

EXPERIENCE AND TECHNICAL SKILLS

• Minimum 6 years’ relevant experience in pharma or academic
• Proven ability to lead and work effectively in a team environment and matrix structure
• Significant experience in clinical research from industry or academia with a preference for antibiotic clinical development
• Experience of working in collaborative research partnerships is desirable
• High level understanding of the ethical and compliance requirements for clinical research
• Ability and experience with drafting clinical study documents including protocols with responsibility for medical /scientific sections.
• Experience with co-leading and working as part of a study operational team
• Has working knowledge of statistics, data analysis, and data interpretation

GENERAL SKILLS AND ATTRIBUTES:

• Has excellent written and oral communication in multicultural, multi-lingual environments. and cross-functional collaborative skills
• Strong ability to work effectively as part of a multicultural cross-functional collaborative teams
• Strong ability to use initiative, prioritize, multi-task, and work well under pressure to meet deadlines
• Clear and systematic thinking that demonstrates good judgment and problem-solving competencies
• Well organized and structured with ability to work independently with minimal supervision
• Strong analytical skills
• Strong ability to provide high level support in project/program delivery
• Strong ability to manage medium/large projects with budget management
• Strong management, negotiation, and advocacy skills
• Strategic thinking and leadership abilities
• Has autonomy for taking actions and decisions
• Strong ability to interact with external stakeholders

EXPERIENCE

• Minimum 6 years’ relevant experience in pharma or academic
• Proven ability to lead and work effectively in a team environment and matrix structure
• Experience of working in private sector and/or public and collaborative research partnerships is highly desirable

EDUCATION

• MD, Ph.D, Pharm.D or graduate degree with equivalent in experience.

Other Requirements

• Fluency in English as the professional working language
• Proficiency in local languages is advantageous
• Very good knowledge of Microsoft Suite

To Apply:

• Please submit your application using the online form
• Deadline for applications: 10.10.2024.
• All candidates will be reviewed after closing date