Project Specialist

premierresearch; Argentina; On-site; ARS 78,757,000 - 118,135,000; Full time

Job summary

Premier Research is seeking a Project Specialist to join our Business Operations team. You will partner with the PM to drive project delivery across cross-functional teams, manage communications, and maintain documentation.

The role includes tracking budgets, invoices, and change orders, ensuring audit readiness, and maintaining study team lists and systems. You will support vendor management, tracking supplies and expenses, and contribute to process improvements in a fast-paced biotech and

Qualifications

• Associate degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or related field with 2+ years clinical research experience, or a Bachelor’s degree with 1+ year in related areas.
• Basic knowledge of ICH/GCP regulations.
• Working knowledge of FDA guidance documents/EU directives/ISO14155 regulations.
• Basic knowledge of project management terminology and guidelines.
• Strong MS Office skills.

Responsibilities

• Partners with the Project Manager to ensure overall Project Delivery through coordination and oversight of the cross-functional project team.
• Facilitates team communications and maintains documentation; manages meeting agendas, minutes, and action logs.
• Tracks budgets, vendor projects, invoices, and change orders; monitors out-of-scope services.
• Tracks supplies and budgets related to vendor management as applicable.
• Ensures projects are audit ready and maintains project systems, SOP indices, and study team lists.

Skills

MS Office proficiency

ICH/GCP knowledge

FDA/EU/ISO regulations knowledge

Project management terminology

Communication and coordination

Education

Associate's degree or Bachelor's in life sciences or related field

Job description

Premier Research is looking for a Project Specialist to join our Business Operations team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

Your ideas influence the way we work, and your voice matters here.

As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing:

• Partners with the Project Manager (PM) to ensure overall Project Delivery through coordination and oversight of the cross-functional project team
• Responsible for facilitating team communications and maintaining documentation internally and externally. Maintains internal and external project team contact lists. Ensures effective communication by scheduling internal and external team meetings, developing agendas, capturing minutes, and managing the action/decision log. Creates and distributes study newsletters as required.
• Manage and track budgets related to vendor projects including tracking of supplies and invoices. Track out of scope services and assists in preparing Change Orders.
• Tracks supplies, invoices, and budgets relating to vendor management, as appropriate.
• Ensures projects are audit ready
• Creates and manages the required project systems, SOP indices, and study team lists, as applicable. Manages study team/contact lists, system access requests, and e-mail distribution lists as required

What we are searching for:

• Associate's degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field and a minimum of 2 years of clinical research experience or a Bachelor's degree, or international equivalent, preferably in a clinical, biological, scientific, business, or health-related field, and a minimum of 1 year of professional work experience in clinical research, healthcare, business, finance, and/or project management preferred
• Basic knowledge of ICH/GCP regulations
• Working knowledge of FDA guidance documents/EU directives/ISO14155 regulations, drug/device development, and clinical monitoring procedures
• Basic knowledge of project management terminology and guidelines
• Strong computer skills in MS office suite requred