Thermo Fisher Scientific Clinical Trials Project Manager in Harrisburg, Pennsylvania
Location/Division Specific Information
CTD partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time - a concept that we internally embrace as 'There is a Patient Waiting.' Our unique blend of services includes project management, packaging, distribution, transportation management and specialty logistics, ancillary supply management, clinical supply optimization, bio-repository storage and much more. Our more than 3000 employees in over 15 countries work hard every day knowing that what they do matters.
How will you make an impact?
As part of our global team, what you do contributes directly to our mission; enabling our customers to make the world healthier, cleaner and safer.
What will you do?
Interface with both the client and internal teams to coordinate packaging activities for a variety of different clients. Follow standard processes that will foster on time delivery of the packaged product. Work with clients and internal groups to continually improve the various processes to improve on time delivery and right first-time output.
How will you get here?
- Accredited college, university or recognized professional degree, preferably in a health-related field.
Manages the delivery of all technical and service aspects of projects and studies for clients.
Determines the preliminary design of the study and evaluates and understands the study.
Serves as the internal link within the company and will have direct contact with all internal departments and direct one on one contact with external customers.
Initiates the involvement of appropriate departments, maintaining continuous communication with those departments, and ensures the work delivered to customers is of a consistently high standard.
Attends Project Meetings at the business or customer site. Leads and represents the business at kick off meetings as required by the customer.
Leads and facilitates customer teleconferences, visits and audits as required, and provides timely provision of customer reports and updates.
Interacts with Quality Assurance/Regulatory personnel to drive Problem Reports to closure.
Ensures customer needs are properly translated into quotation and has responsibility to monitor and amend the quote and budget as required.
Participates in cross-functional business process improvement activities as required.
Works closely together with the account manager to gain overall customer satisfaction.
Applies Good Manufacturing Principles in all areas of responsibility.
Demonstrates and promotes the company vision.
Knowledge, Skills, Abilities
Understanding and competent use of SOPs required by company Quality standards.
3 years of successful experience in clinical trial project management as a Project Manager or Coordinator
In depth understanding of clinical trials.
Excellent organizational, planning, verbal, written and numerical skills with the ability to analyze and define solutions and manage multiple tasks to meet strict deadlines.
Strong and effective communicator with the ability to effectively present information and respond to questions from groups of managers and clients.
Strong interpersonal and communication skills to include excellent relationship building.
Excellent communication, organizational skills and project co-ordination skills.
Ability to develop strong customer management skills; proactively anticipates, understands, and responds to the needs of clients to meet or exceed their expectations.
Knowledge of all internal systems associated with projects (i.e. Salesforce, GPMS, TrackWise).
Proficiency in personal computer applications (e.g. Microsoft Word, Excel, PowerPoint, Access, Outlook).Proficiency in appropriate project planning tools e.g. Microsoft Project to communicate milestones and critical path activities and responsibilities.
Mastery of basic Project Management concepts as a recognized institution in project management.
Proven experience with customers in a dynamic environment.
Mastery of skills required to read, understand, and adhere to the SOPs and policies of a GMP environment.
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com .
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.
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