Posted Position Title BioPharm Project Manager

Job Number	1850706
Business	GE Healthcare
Business Segment	Healthcare Life Sciences
About Us	CLARiENT, a GE Healthcare company At Clarient, we combine innovative diagnostic technologies with world-class pathology expertise to assess and characterize cancer. Our mission is to become the leader in cancer diagnostics by dedicating ourselves to collaborative relationships with the healthcare community to translate cancer discovery and research into better patient care. Our principal customers include pathologists, oncologists, hospitals and biopharmaceutical companies. The rise of individualized medicine as the new direction in oncology has created the need for a centralized resource providing leading diagnostic technologies, such as flow cytometry and molecular testing. Clarient is that resource, with a state-of-the-art commercial cancer laboratory providing the most advanced oncology testing and diagnostic services. We are also developing new, proprietary “companion” diagnostic markers for therapeutics in breast, prostate, lung and colon cancers, and leukemia/lymphoma. We are taking cancer personally. What do you envision for your future? At GE Healthcare, we strive to see life more clearly. Our "healthymagination" vision for the future invites the world to join us on our journey as we continuously develop innovations focused on reducing healthcare costs, increasing access and improving quality and efficiency around the world. We are a $17 billion unit of General Electric Company (NYSE: GE), employing more than 46,000 people worldwide and serving healthcare professionals in more than 100 countries. We believe in our strategy - and we'd like you to be a part of it. As a global leader, GE can bring together the best in science, technology, business and people to help solve one of the world's toughest challenges and shape a new age of healthcare. GE is committed to diversity . We aim to employ the brightest minds in the world to help us create a limitless source of ideas and opportunities . We believe in hiring talented people of varied backgrounds, experiences and styles - people like you … Something remarkable happens when you bring together people who are committed to making a difference - they do! At work for a healthier world. For more information about GE Healthcare join our LinkedIn Group: GE Healthcare Global Community or visit our website www.gehealthcare.com/careers.
Career Level	Experienced
Function	Engineering/Technology
Function Segment	Clinical Development
Location(s) Where Opening Is Available	United States
U.S. State, China or Canada Provinces	California
City	Aliso Viejo
Postal Code	92656-1460
Relocation Expenses	No
Role Summary/Purpose	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The BioPharm Project Manager role oversees the project management for multiple projects within the BioPharm department. In addition, this position is accountable for achieving quality objectives, meeting schedules and effective team execution, as well as communicating project status and escalating issues when appropriate to facilitate transparency. The successful incumbent will be responsible for customer-facing relationship management with the client for whom the project(s) is being conducted.
Essential Responsibilities	Duties include (but are not limited to): Responsible for multiple studies providing the study team with overall direction, clear expectations for deliverables and the leadership necessary for the successful management, conduct, progress tracking, and completion of the study or studies. This includes ensuring project activities and milestones are planned, agreed and achieved according to the specifications outlined by the sponsor. Plans, implements and drives all aspects of studies according to the directions given by the study sponsor and in accordance with Good Laboratory Practice, Standard Operating Procedures, Corporate Policies, Guidelines and internal Standards. Ensuring the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports. Managing, maintaining and accurately forecasting the project team resource requirements, timelines, and ensuring high level of data quality. Provides ongoing communication with the sponsor according to agreed upon schedule. Provides regular status updates to management team
Qualifications/Requirements	Bachelors Degree 4+ years relevant project leadership and project management experience 2+ years experience working in a clinical or diagnostic lab environment or pharma organization Strong familiarity with ISO, GLP, GCP and other related regulatory standards guidelines and SOPs Demonstrated leadership of cross-functional project teams and an ability to drive project design plans to completion Demonstrated interpersonal skills to build good working relationships both internally and externally Ability to work independently and systematically Proven ability to manage complex projects Must be legally authorized to work in the United States full-time Must be willing to work in our Aliso Viejo, CA facility full-time Must be willing to submit to a drug test, and background check – including verification of previous employment, criminal history and educational background Must submit application for employment through gecareers.com (or COS if internal) to be considered Must be 18 years of age or older
Additional Eligibility Qualifications	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics	5+ years experience working in a clinical or diagnostic lab environment or pharma organization Strongly prefer PhD/MS degree in Life Science Excellent skills in written and verbal presentation Experience of biomarker assay development and implementation in clinical trials. PMP (Project Management Professional) certification.