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Clinical Administrative & Project Coordinator

Propharma
Propharma
2-3 years
Not Disclosed
Remote, USA, Remote
10 May 6, 2026
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 Overview

ProPharma Group has over 20 years of experience improving patient health and wellness by supporting biotech, medical device, and pharmaceutical organizations.

Through its advise–build–operate model, ProPharma delivers end-to-end solutions across the product lifecycle, with expertise in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


Role Title

Clinical Administrative & Project Coordinator


Job Details

  • Work Mode: In-office

  • Location: Gaithersburg, MD or Conshohocken, PA

  • Reporting To: VP, Clinical Development


Role Summary

This role provides high-level administrative and project coordination support to senior clinicians within Clinical Development.

The position focuses on:

  • Enabling senior clinicians to prioritize strategic activities

  • Managing schedules and communications

  • Supporting clinical trial-related operations and internal processes

The ideal candidate is detail-oriented, highly organized, and comfortable working in a fast-paced biotech environment while collaborating with diverse stakeholders.


Key Responsibilities

1. Executive Support

  • Provide administrative support to senior clinicians:

    • Draft correspondence

    • Prepare presentations

    • Coordinate cross-functional communications

  • Collaborate with:

    • Chief of Staff

    • Executive Administrator

    • Clinical Development Leadership Team

  • Maintain documentation, policies, and procedures

  • Act as liaison between Clinical Development and other teams

  • Handle sensitive information with confidentiality and professionalism


2. Calendar & Time Management

  • Manage complex calendars for multiple senior clinicians

  • Coordinate:

    • Meetings

    • Calls

    • Interviews

    • Events

  • Align schedules with clinical trial milestones and business priorities

  • Resolve scheduling conflicts and last-minute changes efficiently


3. Meeting Coordination & Follow-Up

  • Prepare meeting agendas

  • Take notes and track action items

  • Ensure stakeholders are prepared with pre-reads

  • Monitor follow-ups and ensure timely execution

  • Facilitate effective communication across teams and projects


4. Travel Planning & Investigator Support

  • Organize complex international travel:

    • Flights, accommodations, visas, transport

    • Expense reporting

  • Support outreach to:

    • Clinical trial sites

    • Investigators

  • Ensure compliance with travel policies and budgets

  • Anticipate needs of senior clinicians


5. Project & Data Support

  • Track:

    • Project timelines

    • Milestones

    • Deliverables

  • Support:

    • Ad hoc data analysis

    • Process improvement initiatives

  • Prepare reports, presentations, and updates

  • Apply project management principles to ensure timely delivery


6. Technology & Workflow Optimization

  • Use tools such as:

    • Microsoft Office (Excel, Word, PowerPoint)

    • CRM systems

    • Project tracking tools

    • AI-enabled tools

  • Improve workflow efficiency and team productivity


Education Requirements

  • Bachelor’s degree (required)

  • Preferred fields:

    • Business

    • Life Sciences

    • Related disciplines


Experience Requirements

Required

  • 2–3 years of experience in:

    • Project coordination

    • Administrative support

    • Analyst roles


Preferred

  • Experience in:

    • Clinical research

    • Biotechnology, pharmaceutical, or healthcare industries

  • Understanding of:

    • Clinical trial processes

    • Regulatory requirements

  • Experience with:

    • Travel and expense management

    • Project management tools

    • CRM systems

    • AI tools


Skills & Competencies

  • Strong organizational and multitasking abilities

  • Excellent written, verbal, and visual communication skills

  • Professional interpersonal skills and stakeholder management

  • Advanced proficiency in:

    • Microsoft Office Suite

    • Calendar management tools (Outlook, Google Calendar)

  • Strong problem-solving and analytical thinking

  • Ability to work independently in a fast-paced environment

  • High attention to detail and confidentiality

  • Positive attitude and willingness to learn


Work Culture & Values

  • Commitment to Diversity, Equity & Inclusion

  • Equal Opportunity Employer

  • Encourages innovation, collaboration, and authenticity

  • Supportive and inclusive workplace environment


Application Process

  • Applications are personally reviewed by the recruitment team

  • No AI-based screening tools are used

  • All candidates receive an application outcome


Important Notice

  • No unsolicited resumes from recruiters or third parties

  • No phone calls or emails regarding this role