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Intelligence and National Security Alliance

Project Manager

Intelligence and National Security Alliance, Morrisville, North Carolina, United States, 27560

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Job Title: Technical Project Manager / Business Analyst - Life Sciences (Patient Engagement Focus) Location: Morrisville, NC

About Incedo Incedo is a digital transformation firm specializing in unlocking the potential of technology to drive client growth. We are seeking an experienced and dynamic Technical Program Manager/Business Analyst with deep domain expertise in Life Sciences, specifically within

Patient Support and Patient Connection/Engagement programs , to lead mission‑critical digital initiatives.

Role Summary The Technical Project Manager/Business Analyst will act as the crucial link between business stakeholders and technical delivery teams. This role requires defining, prioritizing, and managing requirements for digital platforms focused on enhancing patient support, adherence, and communication programs (often referred to as 'Patient Connect' or 'Patient Services'). The successful candidate will drive technical delivery, manage program timelines, and ensure solutions meet strict regulatory standards.

Key Responsibilities Business Analysis & Requirements Management

Lead discovery sessions

with pharmaceutical and medical device clients to elicit, document, and prioritize functional and non‑functional requirements for patient support/adherence programs.

Develop detailed

Business Requirements Documents (BRDs), functional specifications, use cases, user stories, and acceptance criteria

(Gherkin format, where applicable) for digital patient solutions.

Define the product backlog and roadmap

for patient‑facing applications (web, mobile) and underlying data/integration platforms, ensuring alignment with commercial and clinical objectives.

Technical Project Management & Delivery

Manage the full project lifecycle

(initiation, planning, execution, monitoring, and closing) for technical projects involving

Patient Relationship Management (PRM), patient portals, EMR/EHR integration, and consent management systems.

Lead cross‑functional technical teams

(Development, QA, DevOps) using Agile/Scrum methodologies, facilitating ceremonies, and removing roadblocks to maintain velocity.

Oversee technical solution design

to ensure systems are scalable, secure, and compliant, particularly concerning data flow between patient enrollment, case management, and financial assistance programs.

Life Sciences Domain & Compliance

Act as the Subject Matter Expert (SME)

in the Life Sciences domain, focusing on patient support services, including adherence, copay, reimbursement, and nursing support workflows.

Ensure all requirements and implemented solutions adhere to stringent regulatory guidelines, including

HIPAA, GDPR, FDA GxP standards, and 21 CFR Part 11.

Conduct

risk analysis

related to patient data privacy, security, and system validation requirements.

Required Skills & Qualifications

[8+] years of experience

performing Business Analysis or Program Management in the

Life Sciences, Pharmaceutical, or Healthcare

domain.

Mandatory expertise in Patient Support, Patient Connect, or Patient Engagement programs,

including understanding enrollment, benefit verification, adherence, and nurse support services workflows.

Proven ability to define requirements for

CRM/PRM platforms (e.g., Salesforce Health Cloud, Veeva), patient portals, or digital health applications.

Strong technical background with experience managing projects involving

API integration, cloud architecture (AWS/Azure), and data warehousing

principles.

Expert proficiency in

Agile methodologies (Scrum/Kanban)

and using tools like Jira, Confluence, or Azure DevOps.

Exceptional communication, negotiation, and presentation skills, with the ability to articulate complex technical concepts to non‑technical stakeholders.

Preferred Qualifications

Certification in Business Analysis (CBAP) or Project Management (PMP, CSM).

Experience with

data privacy frameworks

beyond HIPAA (e.g., CCPA, GDPR).

Familiarity with clinical trial management systems (CTMS) or regulatory affairs platforms.

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