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Clinical PM (Registries) - Great benefit
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Clinical PM (Registries) - Great benefits, Great e
Position Id
CC-1022 .
Last Updated
1/8/2008 9:23:31 AM .
Type
Permanent .
Minimum Education
Contact
None Specified
recruiter7@ccesearch.com
Description
Clinical Project Manager (Registries) - Great benefits, Great environment, Home Based Opportunity!
Location: Anywhere in the US!
Client Description: Our client is a therapeutically focused Contract Research Organization (CRO) that emphasizes on integrity and innovation. They have emerged as a healthy and growing research firm and offer an excellent environment for success! This specific group within the organization delivers real-world evidence that demonstrates value to their customers and helps products succeed in the market.
Opportunity Statement:
Under the general direction of the Late Phase Vice President, the primary functions of this position are responsible for day-to-day management of Registry programs from Registry design through implementation.
This position relies on extensive late phase clinical research experience that enables the individual to plan, direct and execute all activities required to successfully manage a clinical study.
Responsibilities:
Position responsibilities will include, but not limited to;
Project design, development, production and implementation of various registry programs throughout a project s lifecycle
Full scope project management including client interface, budget and timeline adherence and internal team management
Support on-going business development efforts related to Registry services including participation in presenting to prospective clients and leading proposal development
Design Registry programs and post approval studies in conjunction with sponsors and internal SOP s
Maintain industry knowledge of post approval studies market including study methods, guidelines and practices, and technology; includes conducting research for assessing current Registry practices and future trends
Work cooperatively with internal cross functional departments to meet project goals.
Participate in registry process design
Create and participate in study materials development
Prepare and lead sponsor meetings
Focus on budget development and management
Develop project plans and maintain adherence within
Communicate with clients regarding changes in scope
Report on project status internally and externally
Qualifications
Clinical project management experience with registries, post marketing and prospective studies.
Bachelor's level degree in life sciences, pharmacy, nursing or RN preferred
5+ years of experience in the Pharmaceutical/CRO industry.
Demonstrated experience in project management tasks (e.g., work plans, financial budgets, timelines, status reports, issue management, resource and personnel management) with 3+ years experience in the role of Project Manager
Experience working on a team across multiple functional areas (e.g., work with Quality Assurance, Data Management, Medical Affairs, Finance)
Strong knowledge of clinical trial operations, Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
Demonstrated ability to successfully supervise and lead others.
Excellent communication, relationship building and interpersonal skills.
Excellent organizational skills and ability to prioritize and multi-task.
Proficient in Microsoft Office (e.g., Word, Excel, and Outlook).
Company Benefits: 4+ Weeks of Vacation, Fantastic Health Benefits that kick in immediately, Immediate 401K enrollment with 24 Month Vesting Period and Matching, Semi-Annual Salary Increase Opportunities, Work from Home and Amazing Growth Potential!!!
Characteristics:
Self starter and the ability to work with minimal supervision
Passion, energy, personal drive and motivation
Outstanding leadership and communication skills are required
Excellent verbal and written communication skills
Ability to multi-task, meet rigorous timelines and be a proactive problem-solving skills
Proficient computer skills, with ability to learn other applications as needed
As a professional search firm, we will only be responding to those inquiries that most closely align with the stated requirements. Please include the position ID (CC1022) in the subject line of your correspondence to ensure review and forward your credentials (*Word format please), in confidence, to: recruiter7@ccesearch.com.
General CV/resume submissions for inclusion in our knowledgebase of future opportunities can be made to: resume@ccesearch.com
For our most recent searches, please review our web site at: www.ccesearch.com
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Applicant Category: Professional
Requisition Code: Work at home
Two Initials of Recruiter: bw
System Date: 01/21/2008
System Time: 13:33:24
Document Name(40): Clinical PM (Registries) - Great benefit
Source: MRINetwork - USA
SearchTerms: "work at home" "work from home"
URL(80): http://www.mrinetwork.com/pcrbin/positions.exe?action=details&p..job_id=20379927
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