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Job Details

Site Manager – ED&CP – Master

Company: Docs Global (Continental Europe)
Location: Madrid,Spain
Reference: Ref AS-017122
Closing Date: 05 Dec 16
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

Why join DOCS? If you are an experienced clinical proffesional looking for an opportunity with a rapidly growing and fast paced global leader on an interesting and complex project, this would be a compelling role for you. To express your interest, please reply to this role and a DOCS Recruitment specialist will contact you to discuss the position in detail.

Requirements:

Roles & Responsibilities of the position

A Site Manager is the person in Trial Co-ordination and Site Management that serves as primary contact point between the sponsor and the investigational site.
A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock.
Responsibilities include site selection,pre trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out.

Job Requirements

A minimum of 1-2 years experience monitoring oncohematology or oncology trials, phase I-II trials are preferred

Should have solid understanding of the drug development process including ICH/GCP and local regulatory requirements.
Preferably with experience in Early Development and Clinical Pharma.

Communication skills: Capacity to persuade, convince and encourage others to contribute or support the objectives.. The candidate should have strong communication skills.
Also act with initiative taking the lead of his work proactively and autonomously.
Analysis and Problem solving: Ability to take initiative and autonomy to look for and manage necessary information to respond to the problems and difficulties to perform their work, offering appropriate solutions.
Ability to identify risk and trends required. Data analysis and technical skills in the area of clinical trials/clinical data is required.
Flexibility and proactiveness.
Motivation and learning: Interest in learning new things and learn or deepen the knowledge acquired. The candidate must be aware of opportunities to learn and look for them proactively.
Proficient in speaking and writing English language

Remuneration & other details

Attractive salary and challenging project.
Partially homebased.

Apply for this job: Site Manager – ED&CP – Master

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

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