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Job Details

Clinical Trial Project Manager

Company: Hobson Prior
Reference: HR444659
Closing Date: 14 Mar 17
Type: Permanent
Salary (£): On Application
Benefits: 35000

Job Summary:

Represents as the client's primary point of contact, at all times maintaining a high level of customer service and satisfaction, displaying precision in delivery and flexibility in approach.


Key Responsibilities:

Represents as the client's primary point of contact, at all times maintaining a high level of customer service and satisfaction, displaying precision in delivery and flexibility in approach.

After training period is complete, manage from 10 to 25 protocols, depending on scope and complexity (managing above $3,000,000 in contract value and maintaining more than 120 PM billable hours per month).

Review clinical protocols and assist with protocol set-up functions as required.

Develops the Global Laboratory Specification Document, Investigator Manual, and protocol specific Global Work Practice Instructions.

Participates and documents Quality Audits and inspections of Clinical Trials as prescribed by departmental policies and regulatory agencies.

Evaluates and communicates monthly project metrics and analyses all activity related to the trial, including monthly budget review.

Conducts investigator training sessions by telephone or at investigator meetings, which involves overnight travel, frequently on weekend days.

Is able to travel to client events (training, bid defenses, Investigator Meetings) and the companies international locations, requiring overnight travel, as well as passport qualifications

Assumes full responsibility for study conduct on behalf of the companyy, ensuring client goals and timelines are met and performs troubleshooting and problem solving functions as the need arises.

Responsible to take On-Call coverage duties as assigned.

Assumes responsibility for regulatory required study documentation and complies with standard procedures for collecting, maintaining and then archiving the materials in accordance with regulations, company policies and client contractual clauses.

Develops protocol specific procedures as needed.

Performs duties with a general working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations, as pertains to central laboratory functions.

Understands and follows company policies and procedures while always maintaining patient and client confidentiality, both inside and outside of the work place.


Minimum Qualifications:

Bachelor's degree required, or 5 years relevant experience and must be matriculated. A degree in a health care or scientific concentration is preferred.

Two years of Health Care related experience OR a minimum of twelve months of project management experience required.

Required Licensure / Certification Skills:

Rochester Regional Health System is an Equal Opportunity / Affirmative Action Employer. Minority/Femal/Disability/Veteran





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Contact Information:

Address:  Hobson Prior International Ltd
Wellington Gate
7-9 Church Rd.
Tunbridge Wells
Tel:  01892 612 612
Fax:  01892 612 613
Website:  Visit Our Web Site

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