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Direct Portfolio Project Manager (Admin) — Pharmaceutical (Remote/Onsite – Indianapolis, IN) Contract

Remote:

Full Remote

Contract:

Fixed term

Experience:

Mid-level (2-5 years)

Work from:

Indiana (USA), United States

Offer summary

Qualifications:

3+ years in clinical trial project management, Strong knowledge of clinical trial protocols, Experience in patient recruitment strategies, Excellent project management and communication skills.

Key responsabilities:

Develop and implement patient engagement strategies
Manage trial-related projects ensuring compliance
Collaborate with internal teams to improve processes
Assist with administrative project support

Pharmavise Corporation http://www.pharmavise.com

11 - 50 Employees

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Job description

This is a remote position.

Our Fortune 500 Pharmaceutical client has an exciting opportunity for Direct Portfolio Project Managers.

Job Summary:
We are seeking experienced Direct Portfolio Project Managers to support a project with one of our clients in their Clinical Trials Patient Engagement Team, driving innovative strategies to enhance patient involvement in research. This role plays a critical part in optimizing clinical trial recruitment, retention, and overall project management. The ideal candidates will have a strong understanding of clinical trial processes, protocols, and regulatory best practices, combined with expertise in project management.

We have three (3) open positions, focusing on Project Management with light administrative support.

Key Responsibilities:

Recruitment & Retention Strategy: Develop and implement strategies to enhance patient recruitment and retention for clinical trials and programs.

Project Management Oversight: Provide leadership in managing trial-related projects, ensuring efficiency, compliance, and adherence to regulatory requirements.

Cross-Functional Collaboration: Work closely with internal teams and stakeholders to streamline clinical processes and improve trial outcomes.

Administrative Project Support: Assist with administrative tasks related to project coordination and execution.

Qualifications :

Minimum of 3+ years of experience in clinical trial project management, patient engagement, or related fields.

Strong knowledge of clinical trial protocols, processes, and regulatory best practices.

Proven experience developing and executing patient recruitment and retention strategies.

Excellent project management, organizational, and communication skills.

Administrative and coordination experience in clinical project settings.

Familiarity with regulatory guidelines related to clinical trial operations.

Other Details :
·        Schedule: Full time, 40 hours per week
·        Contract Length: 18 months with renewal
·        Work Setup: Indianapolis preferred, but will consider remote for very strong candidates
·        Resources Needed: 3

E-Verify Participation :

Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.