Project Manager - Bethesda, United States - CAMRIS International

Description

Overview

We are seeking a Project Manager to support the National Institutes of Healths National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, MD. Our NIAID professional, technical, and scientific support personnel are part of a team focused on positively impacting millions of lives around the world. Candidates will work at a diverse and vibrant NIAID worksite to directly support ongoing research activities as a contractor team member. Take the next big step in your career and apply below to help us make a difference.

CAMRIS International is a dynamic clinical research and international development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with todays most effective, evidence-based best practices. Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.

Our employees enjoy a diverse, collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.

Responsibilities

• Manage, coordinate and facilitate the development of the project plan for the development of vaccines and therapeutics, apply a general knowledge and understanding of the pharmaceutical product development process, particularly as pertinent to biologics and vaccines. Facilitate agreement among team members on the specifics and adequacy of the plans intermediate goals and objectives and the scheduling for completion of tasks.
• Serve as a resource, apply a general knowledge and understanding of the pharmaceutical product development process, particularly as pertinent to biologics and vaccines, to the design and conduct of projects where the specifics of the project are difficult to determine in advance. Provide recommendations and seek guidance on solutions to advancing the project and/or methods used.
• Work with the team to develop or refine solutions to problems that have significant impact on existing program policies and/or procedures. Anticipate major problems and works with the team to identify future program needs to accomplish the programs mission.
• Monitor and assess the status of projects as they progress; use critical path analysis and/or comparable project management tools to track progress; monitor deadlines and other benchmarks to ensure that VRC activities are meeting stipulated obligations.
• Identify current or emerging issues affecting the project tasks/activities and/or the accomplishment of its scientific objectives, the sequencing of activities, activity completion times, etc. Disseminate information to the team on the status of the activities, issues/problems, emerging schedule conflicts or opportunities to accomplish the work.
• Apply knowledge of the pharmaceutical product development process to guide team meetings and other interactions in order to clarify critical problems, to develop proposed solutions to problem or issues, to resolve gaps in skills or capacity needed to accomplish the work, to assess options and their impact on the projects costs, quality of work products and timeliness of completion of tasks, etc.
• Facilitate the resolution of conflicts among the teams members who represent different organizational groups with varying interests or concerns that may conflict with the projects timetables, scientific requirements, availability of staff and/or staff time, available resources, sequencing demands, etc. Elevate conflicts when necessary to resolve project issues.
• Apply situationally appropriate project management practices to guide teams to successful completion of the project, to keep activities on schedule and to facilitate an effective project that best meets VRC and NIAID goals. Seek out guidance to bring back to the team members collectively or individually.
• Continuously collaborate with the VRC managers, laboratory heads, principal investigators, and other personnel to identify, devise, implements and maintain improvements in the management of vaccine development and manufacturing projects.
• Serve as the teams information manager. Originate, formulate, and disseminate project information, assessments and evaluation to assure that team members are properly apprised of progress and that members views concerning the project activities are properly disseminated in order to integrate project activities across the team.
• As assigned by the Director of Project Management, manage VRC inter-agency, academic, and industrial agreements, including preparation of work plans, collate technology transfer documentation, organize agreement activities, and provide guidance to VRC on requirements and activities.

Qualifications

• Bachelors degree in the life sciences. Masters degree, preferred.
• Minimum of 5 years of experience in the pharmaceutical, vaccine, biologics, or similar industry is required.
• At least three years of experience in R&D, product development, or GMP manufacturing is required. Experience advancing Phase I/II products to clinic is preferred.
• Must have experience working in a product development environment, with participation on a cross-functional project team. Greater than 2 years experience in project management is preferred.
• Must have experience managing both scientific and organizational information.
• At least two years experience is required in coordination and planning activities on a biologics or vaccine project.
• Alliance management experience is an asset but not required.
• Possess project management skills and ability to synthesize project workloads for vaccine and antibody-based development from Research through Phase I and Phase I clinical trials.
• Must have experience using project management software and ability to distill highly technical information into effective meeting presentations.
• Government contracting experience (SOW writing, technical oversight, financial planning, etc.) is preferred.

CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.

Some positions or sites may require that the incumbent be fully vaccinated against COVID-19. Proof of vaccination may be required.

Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.