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Clinical Development Consultant

Eingestellt von Radiant Info

Gesuchte Skills: Client, Consultant

Projektbeschreibung

JOB DESCRIPTION:

PURPOSE:

The CDC is the primary interface between Client and investigators in aspects of Clinical Research. He/she partners with the TPO on interactions with investigators. The CDC is responsible for new sites prospecting, for site identification and site selection during the FPA process. The CDC is accountable for delivering all regional, local, and corporate portfolio commitments/milestones for sites and trials within responsibility.

KEY RESPONSIBILITIES:

DELIVERY:

Study feasibility, site feasibility, site identification (with CRPs) and site selection -Clinical studies and Observational Research

Deliver all regional, local, and corporate portfolio commitments/milestones for sites and trials within responsibility

Support local needs of globally outsourced studies within responsibility

Manage IITs

OPERATIONAL EXPERTISE

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Regulatory submissions, in affiliates where this is managed by Clinical Operations
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Manage the allocation of patients within the geography

- Manage Site enrollment performance
- Assist sites in recruitment planning
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Develop site level risk plan for enrollment
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Utilize available tools to assess site performance
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Collaborate with TPO CRA to enhance site performance

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Ensure the site ACDD (Anti Corruption Due Diligence) process is followed and maintain appropriate Anti Corruption certification of sites on file

RELATIONSHIPS AND BUSINESS DEVELOPMENT:

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Primary interface with investigators
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Manage the link between site and the TPO
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Collaborate with Client partners, Quality, and other study team members to resolve/escalate site specific issues when necessary
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Contribute to and partner with the local medical organization to deliver on department goals
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Manage and develop strategic relationship with current and future investigators
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Potential new sites-prospecting -seeking opportunities to widen future sites with Client portfolio needs
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Look for opportunities for Portfolio sites, Investigator Networks and Site Management Organizations (SMO)

MINIMUM QUALIFICATION REQUIREMENTS:

PREREQUISITES:

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Master of Science or equivalent
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Knowledge of or experience of the local Healthcare system/model
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Local language
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Should be based in the country/Area where they work
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Willingness to travel to sites(appr. 60%)
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May be field based as per local policies

TECHNICAL:

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Deep scientific understanding/Therapeutic Area knowledge
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Strong, technical, operational Clinical Operations Expertise
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Appreciation of local business and CDO organisation
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Fluent in English

BEHAVIOR/LEADERSHIP SKILLS:

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Work autonomously

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Team player
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Strong interpersonal skills - emotional intelligence
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Learning agility
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Influencing skills -negotiation skills
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Act proactively within responsibility
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Good communication skills (written and orally)
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Conflict resolution

Projektdetails

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Radiant Info