(Senior) Clinical Scientist – Neurology / Rare Disease

(Senior) Clinical Scientist – Neurology & Rare Disease

Location: France or UK
Flexible: Hybrid model – flexible on candidate

About the company –

This well recognised mid-sized and expanding pharma company has been growing year on year thanks to their commitment to fast decision-making processes and their focus on the patients benefit. With commercialised products and heavy investment into their R & D programmes this company is well established to help consistent career progression, and for all their employees to add amazing value to the patients

They are looking for a (Senior) Clinical Scientist who can see multiple products through the Clinical Phases. As a culture they value personal development, cross-functional work and a high degree of care for the patient.

Location – France or UK

Flexibility – Hybrid working available. Average time in office is 2 days a week, however this has been customised to better fit their employees. If based outside of France or UK, you would only be expected to come in for meetings with senior staff members

The Role:

As (Senior) Clinical Scientist, you will play a crucial role in both the development and execution of the Clinical & Medical Strategy. While conducting scientific literature research, competitive analysis you will also be supporting the Medical Development Director and Medical Monitor to add critical value to the Clinical trials.

Responsibilities:

• Take a key role in leading or participating in the marketing and Clinical advisory panel, along with data monitoring, steering committees, and investigator meetings.
• Become the expert on Scientific Clinical Development, able to offer advice to leader and the project teams for the Phase I-IV clinical Trial development.
• Assist in the development of clinical studies and reviewing of the clinical protocols, and clinical study reports for scientific and operational accuracy.
• Participation in Drug Safety Surveillance
• Lead the team in the execution of clinical studies from the medical development perspective

About you:

• Scientific degree (MSc, PhD for example)
• Around 5 years experience of Clinical Research from the pharma industry, or a Pharmaceutical focused CRO
• Ideally experienced in submissions of IND/CTX/NDA/MAA, and interaction with regulatory authorities
• Experienced in the design and execution of Phase I-III Clinical trials, with some late-stage development research
  • Ideally coming from a Neurology or Rare Disease background