Protocol and Clinical Program Excellence Director CV-Library Protocol and Clinical Program Exce[...]

Scienceabode; London; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A leading healthcare research company seeks a Protocol & Clinical Program Excellence Director for a hybrid role in London. This pivotal position provides strategic and operational support for clinical programs. Candidates should hold an advanced life sciences degree and possess over 5 years experience in clinical research, with strong negotiation and communication skills. The position offers a competitive rate of £500-£570 per day.

Qualifications

• More than 5 years of experience in clinical research or drug development.
• More than 3 years involvement in conducting clinical trials.
• Strong skills in written and verbal communication.

Responsibilities

• Develop harmonized processes for the C-ISRC.
• Engage with external stakeholders in clinical development.
• Support enhancement of clinical development approaches.

Skills

Interpersonal skills

Negotiation skills

Conflict resolution

Influencing skills

Fluent English

Education

MD or advanced degree in life sciences

Job description

Protocol & Clinical Program Excellence Director
Contract Length – 12-18 months
Rate – £570/day via Umbrella only
Hybrid from London office

Overview

The Protocol & Clinical Program Excellence Director will provide strategic, scientific planning and operational execution support to the Head Protocol & Clinical Program Excellence to deliver on the CD program excellence goals aligned with the overall CD strategy and vision. The role will support the scientific and operational activities of the CD Central Integrated Scientific Review Committee (C-ISRC) and work closely with the Head Protocol & Clinical Program Excellence, C-ISRC Leads, CD(M)Ds and trial teams, as well as cross functional partner functions as needed. This role is based in the UK / London and in a hybrid working approach.

Job Description

Provides scientific and operational support to the Central Integrated Scientific Review Committee (C-ISRC), supporting, as requested, the Head Protocol & Clinical Program Excellence with the review of Clinical Development Plans (CDPs) and Key clinical documents (Study protocols, DMC charters, etc), to maintain high levels of quality and consistency across the therapeutic areas.

Responsibilities

• Develops harmonized processes, tools and resources to enable a seamless C-ISRC process
• Supports and acts as delegate to the Head Protocol & Clinical Program Excellence in activities like interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards etc.) and internal NVS stakeholders as needed.
• Supports enhancement and simplification of the clinical development approach (CDP, clinical trial designs, protocol and its review) to improve speed and outcome success of clinical programs.
• Engages the CD(M)Ds and the broader CD community around clinical learnings across therapeutic areas. Supports the CD talent step-up strategy. Supports strategic directions for professional CD capability building.
• Supports the Head Protocol & Clinical Program Excellence to build cross-function collaborations and initiatives leading to a step-wised transition to the futuristic digital clinical trial era.

Education and experience

• MD or advanced degree in life sciences/healthcare (or clinically relevant degree) is required. PharmD, or PhD strongly preferred
• More than 5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
• More than 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry
• Excellent interpersonal, negotiation, conflict resolution verbal and written communication skills
• Strong skills at influencing without formal authority
• Fluent oral and written English

Carbon60, Lorien & SRG – The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy

£500 – £570/day

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