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0-3 years
Not Disclosed
10 Nov. 22, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Description

Katalyst HealthCares & Life Sciences is actively hiring entry-level candidates for various positions in contract research focused on clinical trials of drugs, biologics, and medical devices. We collaborate with university hospitals, pharmaceutical companies, and recruiting partners to offer career opportunities in Drug Safety, Pharmacovigilance, and Clinical Research.


Job Description

Position: Project Management Support - Client Devens, MA

We are seeking a motivated entry-level candidate to join our Project Management Office for a 6+ month contract role. The successful candidate will play a crucial role in delivering technical projects across the 350+ person site. This role requires a demonstrated background in bioprocessing (upstream and/or downstream) and strong communication skills to manage project deliverables and coordinate cross-functional teams.


Responsibilities

  • Collaborate with project leaders and cross-functional teams to provide support on projects related to upstream/downstream processes, Quality, Supply Chain, Automation/IT, Manufacturing Technologies, Technical Services, and more.
  • Develop project plans with the project team, sequence activities, facilitate discussions to estimate resource needs and durations.
  • Manage project schedules by reconciling completed and pending activities, and proactively communicating upcoming tasks to project team members.
  • Aggregate and interpret project data to align with the project leader and sponsor, taking necessary actions to enhance team performance. Escalate issues when appropriate.
  • Facilitate team meetings by scheduling, preparing materials, and documenting decisions and actions.
  • Prepare materials for Devens project steering committee meetings and/or network-wide management discussions.

Qualifications

  • Bachelor's or Master’s Degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biochemistry, or a related field (Advanced degree is preferred).
  • 0 - 3 years of experience in process development, process validation, or manufacturing support within bioprocessing (upstream and/or downstream).
  • Preferred: Experience in managing projects and a willingness to learn project management best practices.

Additional Information

All candidate information will remain confidential in accordance with EEO guidelines.