Contract Research Proposal Manager PDF
Transcription
Contract Research Proposal Manager PDF
Date: May 19th, 2015 Contract Research Proposal Manager for PhenoPath’s Contract Research Organization PhenoPath Laboratories, PLLC, is a physician-owned specialty pathology practice and reference laboratory providing diagnostic and contract research services to pathology and oncology practices, hospitals, biopharmaceutical companies and research institutions in the U.S., Canada and around the world. Purpose of the Position The Contract Research Proposal Manager develops and maintains project proposals, plans and scope of work documents for effective coordination and communication with clients, and PhenoPath laboratory staff and management; provides PhenoPath clients and management team with project reports. The CRO Proposal Manager manages all aspects of contract research projects proposals including discussing work requirements with clients, preparation of the Scope of Work documents and study plans, and developing cost estimations quotation. The CRO Proposal Manager works collaboratively with a diverse group of internal and external stakeholders which includes clients’ investigators, scientists and project managers, and PhenoPath pathologists, project managers, business development and sales and marketing, laboratory staff and other experienced team members to ensure that proposals are accurate and in accordance with the client’s requirements. Position Responsibilities and Accountabilities to include Reporting to the CRO Department Manager, the core functions and responsibilities of the position will include but are not limited to: • • • • • • • • • Lead the proposal writing process Prepare the Statement of Work (SOW) documents for clients and/or internal study plans Develop and maintain systems for effective communication within the company to ensure projects/studies contracts are prepared efficiently and accurately Ensure that client satisfaction is achieved through on-time delivery of the proposals. Address client comments with the CRO team Contribute in the writing of the protocol-specific laboratory manuals, study reports, and SOPs Create training materials and protocol specific documents for investigators and internal staff Contribute in the technical writing to support marketing efforts Maintaining study status in CRO database Interface with CRO management, project management, data management, laboratory, sales and marketing personnel • • • • • Assist the CRO management and project management to ensure appropriate communication channels with the Sponsors and Investigators are maintained Update project status to CRO manager Assure new clinical test validations are completed and documented prior to specimen receipt and reporting for specific project Attend study initiation (“kick-off”) meetings Participate in internal quality assurance unit Qualifications and Experience • • • • • • • • • Bachelor’s degree in Biology, Life Sciences, or a related science MT, HTL, or QIHC Certifications In-depth knowledge of clinical trials in Contract Research Organization (CRO) and/or (bio)pharmaceutical settings Demonstrated Project Management skills and ability to meet deadlines Excellent ability in planning research projects Excellent communication, interpersonal and organizational skills with a demonstrated ability to work collaboratively as a member of a team Outstanding interpersonal skills for effective interactions with all levels of the company and with clients Excellent written and verbal communication skills with a dedication to accuracy and attention to detail Proficient with MS Office suite To Apply Please Email: [email protected] Please no phone calls regarding this position from candidates or recruiters.