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Job Details

Clinical Site Manager II

Company: ProClinical Ltd
Location: London
Reference: CR.TS.14833
Closing Date: 22 Jan 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

ProClinical is currently recruiting for a fantastic opportunity within a Global organisation that is seeking an experienced SCRA who is looking to add to their responsibility and grow their career. This is a permanent position to be based in London. Role Overview:The Clinical Site Manager (CSM) is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. ...

Requirements:

ProClinical is currently recruiting for a fantastic opportunity within a Global organisation that is seeking an experienced SCRA who is looking to add to their responsibility and grow their career. This is a permanent position to be based in London.

Role Overview:

The Clinical Site Manager (CSM) is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to initiation, the development of a robust patient recruitment strategy, setting up a system, assessing compliance with regulations and the site’s capability to comply with the study needs and recruitment expectations, and problem solving to address and resolve site issues.

This may include various tasks and roles within the CSM framework, contingent upon project phase and country demands, and complexity of the study. The Clinical Site Manager will oversee the conduct of the trial at designated sites, ensuring the rights and well-being of human subjects are protected, evaluating the quality and integrity of the reported data, evaluating the site efficacy of staff training and requiring retraining where necessary, developing strategy regarding patient recruitment, evaluating and building the relationship with the clinical site, using problem-solving to promote positive working relationships with the site and staff, and ensuring the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP and with the applicable regulatory requirement(s).


Skills and Requirements:

* Strong problem-solving skills.
* Able to take initiative and work independently, and to proactively seek guidance when necessary.
* Excellent presentation skills.
* Client focused approach to work.
* Ability to interact professionally within a client organization.
* Flexible attitude with respect to work assignments and new learning.
* Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
* Strong ability to make appropriate decisions in ambiguous situations.
* Willingness to work in a matrix environment and to value the importance of teamwork.
* Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
* Excellent interpersonal, verbal, and written communication skills.
* Sense of urgency in completing assigned tasks and ability to assist others to meet study/ country deliverables.
* Excellent time management in order to meet study needs, team objectives, and department goals.
* Proven ability to work across cultures.
* Shows commitment to and performs consistently high-quality work.
* Ability to successfully work in a (‘virtual’) team environment.
* Consulting Skills.
* Able to accommodate travel time requirements, according to tasks allocation/phase of the study assigned.
* Act as a mentor and role model for other team members.
* Effectively enlist the support of team members in meeting goals.
* Attention to detail.
* Holds a driver’s license where required.
* Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
* Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Apply for this job: Clinical  Site Manager II

Contact Information:

Address:  ProClinical Ltd
Eldon House Eldon Street London
EC2M 7LS
England
Tel:  0800 988 4437
Fax:  +44 (0)207 834 9470
Website:  Visit Our Web Site

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