Associate Project Manager

Posted 4 Days Ago
Be an Early Applicant
Exton, PA, USA
In-Office
Junior
Healthtech • Biotech • Pharmaceutical
The Role
The Associate Project Manager plans and manages clinical trial projects, ensuring timely completion and collaboration with various departments and clients. Responsibilities include tracking project progress, preparing proposals, and supporting management and business development.
Summary Generated by Built In

                                                                                   Associate Project Manager

 

Title: Associate Project Manager

 

Location: Exton, PA

 

Reports to: Senior Project Manager, Central Lab

 

Full-time

 

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China.  Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position/Job Summary: Plan, execute, manage, and close clinical trial projects.

Roles & Responsibilities

  • Manage and monitor project progress and timelines to ensure successful completion.
  • Participate and communicate effectively in project meetings with clients on a regular basis as well as with internal departments to ensure projects are met with quality and within the applicable scope and budget.
  • Collaborate with financial sector throughout various stages of projects (invoices and revenue recognition).
  • Prepare and review proposals.
  • Generation of clinical trial related documentation as needed and per client request.
  • Support Management and Business Development teams with new business opportunities.
  • Maintain a general working knowledge of phase I-IV clinical trials, FDA regulations/ICH guidelines and other pertinent regulations.

 

Education, Experience & Skills Required:

  • Associate Degree or higher.
  • Has at least 2-3 years’ experience in a clinical laboratory, CRO, or pharmaceutical environment.
  • Has previous project management experience.
  • Excellent communication skills.
  • Proficient with Excel, Word, PowerPoint, Microsoft Teams, and other computer skills.
  • High level of accountability with self and others.
  • Hands-on approach with a desire to teach others.
  • Track record of challenging the status quo.
  • Team and action oriented.
  • Problem-solving.
  • Able prioritize workload.

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Skills Required

  • Associate Degree or higher
  • 2-3 years' experience in a clinical laboratory, CRO, or pharmaceutical environment
  • Previous project management experience
  • Excellent communication skills
  • Proficient with Excel, Word, PowerPoint, Microsoft Teams
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The Company
HQ: Exton, PA
591 Employees
Year Founded: 2001

What We Do

Frontage Laboratories, Inc. is a CRO that provides integrated, science-driven, product development services throughout the drug discovery and development process to enable pharmaceutical and biotechnology companies to achieve their development goals. Comprehensive services include drug metabolism and pharmacokinetics, analytical testing and formulation development, preclinical and clinical trial material manufacturing, bioanalysis, preclinical safety and toxicology assessment and early phase clinical studies. Frontage has enabled many biotechnology companies and leading pharmaceutical companies of varying sizes to advance a myriad of molecules through development and file regulatory submissions in the United States, China and other countries.

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