Clinical Research Lead

Flexsis; Basel; Vor Ort; CHF 140.000 - 190.000; Vollzeit

Zusammenfassung

Flexsis, on behalf of Novartis in Basel, seeks a reliable and motivated Clinical Research Lead (m/f/d) to steer protocol development and cross-functional study execution. The role focuses on authoring protocols, amendments, and contributing to regulatory documents, with a priority on timely, robust study delivery.

Applicants should have a life sciences background with at least 6 years in clinical trials, strong interpersonal skills, and a proven ability to manage complex projects in a global

Qualifikationen

• Bachelor in life sciences; advanced degree preferred.
• Approximately 6+ years’ experience in clinical trials development.
• Strong interpersonal skills and collaboration across functions.

Aufgaben

• Lead clinical protocol development with the Medical Lead and other line functions; responsible author for clinical protocols and amendments.
• Develop strategic and scientific input into study concepts, feasibility, and execution plans with cross-functional partners.
• Collaborate with key partners to identify sites and ensure recruitment commitments.
• Lead a global cross-functional team to meet trial deliverables and timelines.

Kenntnisse

Clinical trial management

Cross-functional collaboration

Project planning

Interpersonal skills

Problem solving

Ausbildung

Bachelor in life sciences

Advanced degree preferred

Jobbeschreibung

Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.

For our client Novartis in Basel, we are looking for a reliable and motivated (m/f/d).

Clinical Research Lead

End date: 31/08/2027

Extension: possible

MAJOR ACCOUNTABILITIES & RESPONSIBILITIES

• Lead the clinical protocol development process in collaboration with the Medical Lead and other line functions; responsible author for clinical protocols, amendments, etc.; contribute to the medical/scientific input given for the development of study-related documents and processes which resides in other line functions; contribute to the development of clinical sections of study-level regulatory documents.
• Lead development of strategic and scientific input into study concept, feasibility, and ability to execute; develops and implements study-level operational execution plan in partnership with key cross functional partners, if applicable.
• Collaborate with key cross functional partners to identify and select strategic and high performing sites to ensure recruitment commitments are met.
• Lead a global cross functional CTT to ensure all trial deliverables are met; sets stretch goals, promotes realistic planning and timelines, and presents actionable alternatives to accelerate timelines.

QUALIFICATION & KEY COMPETENCIES

• Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters). Years of Experience: Key Competencies:
• Approximately 6+ years’ experience in clinical trials development.
• Demonstrates strong interpersonal skills with a proven track record of building strong positive relationships.
• Demonstrates strong tolerance for ambiguity, willingness to adapt, and willingness to speak-up and challenge.
• Embraces a culture of diversity, inclusion, quality, innovation and always driving forward with integrity.
• Proficient in clinical trial methodology with a strong emphasis in early clinical development. Strong operational project management experience including excellent planning, prioritization, problem solving and organizational skills.