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Medical Information Associate Jobs in Basking Ridge, NJ

Flywheel Partners

Medical Writer

Manhattan, NY · Remote

$65K - $85K/yr

Research, learn, and simplify complex scientific/medical information, ensuring it is clearly ... Please inform the Associate Director, Operations if you need assistance completing this application ...

Braze

IT Associate

New York, NY · On-site

$75K - $80K/yr

WHAT YOU'LL DO Braze is seeking an Information Technology Associate to join our team to provide ... Comprehensive benefit plans covering medical, dental, vision, life, and disability * Family ...

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How much do medical information associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for medical information associate in Basking Ridge, NJ is $30.41, according to ZipRecruiter salary data. Most workers in this role earn between $20.34 and $36.15 per hour, depending on experience, location, and employer.

What does a medical information associate do?

A Medical Information Associate is responsible for providing accurate, up-to-date, and unbiased medical and scientific information to healthcare professionals, patients, and internal stakeholders. They respond to inquiries about pharmaceutical products, ensure compliance with regulations, and document all communications. Their role often includes reviewing medical literature, preparing standard response documents, and supporting pharmacovigilance by identifying and reporting adverse events.

What are the key skills and qualifications needed to thrive as a medical information associate, and why are they important?

To thrive as a Medical Information Associate, you need a background in life sciences, strong analytical skills, and familiarity with medical terminology, often supported by a relevant degree. Expertise in databases, pharmacovigilance systems, and regulatory compliance tools, as well as experience with medical writing software, is typically required. Excellent communication, attention to detail, and the ability to manage multiple tasks are crucial soft skills in this role. These skills ensure the accurate dissemination of medical information, compliance with regulations, and effective support to healthcare professionals and patients.

What are some common challenges faced by medical information associates when responding to healthcare professional inquiries?

Medical Information Associates often encounter challenges such as addressing complex or nuanced clinical questions from healthcare professionals while ensuring all responses are compliant with regulatory guidelines and company policies. They must balance providing accurate, evidence-based information with the need for timely responses, often under tight deadlines. Additionally, managing high inquiry volumes and staying updated on new product data and therapeutic areas are regular parts of the role. Strong communication skills and attention to detail are essential for navigating these challenges effectively.

What is a medical information associate?

A medical information associate is a professional responsible for providing accurate, up-to-date medical and product information to healthcare providers, patients, or internal teams. They often review scientific data, ensure compliance with regulations, and may use tools like medical databases or CRM systems to support communication and documentation.

What are the most commonly searched types of Medical Information jobs in Basking Ridge, NJ?

The most popular types of Medical Information jobs in Basking Ridge, NJ are:

What cities near Basking Ridge, NJ are hiring for Medical Information Associate jobs?

Cities near Basking Ridge, NJ with the most Medical Information Associate job openings:

Medical Information Associate jobs near you
Infographic showing various Medical Information Associate job openings in Basking Ridge, NJ as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $63,244 per year, or $30.4 per hour.

Associate Director, Project Management - Medical Affairs (Princeton, NJ or Palo Alto, CA)

Summit Therapeutics

Princeton, NJ • On-site

Full-time

Posted 8 days ago

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role:
The Associate Director, Medical Affairs Project Management role will be critical in ensuring operational excellence, cross-functional coordination, and launch readiness via project leadership of the Global Medical Affairs functional plans.
Reporting to the VP of Project Management, this position serves as a strategic partner to the Medical team while serving as the primary cross-functional operational contact and liaison for effective alignment, communication flow, and governance. The role will serve as a central point of contact for operational planning, delivery, and governance of critical Medical Affairs projects-spanning scientific communications, congress strategy, advisory boards, medical education, and post-marketing data generation supporting launch preparation.
This role focuses on day-to-day project execution, ensuring defined scope, timelines, budgets, and quality objectives are met across the commercial product lifecycle.
Role and Responsibilities:
Strategic Project Leadership and governance
    • Lead cross-functional medical planning and execution for launch readiness sub-team/s, integrated evidence generation plans, scientific platform development, and field medical enablement.
    • Define and oversee medical workstreams for new product launches, indication expansions, and lifecycle management.
    • Establish and maintain dashboards, KPIs, and governance frameworks to monitor progress, identify risks and develop mitigation solutions, and drive accountability.
    • Facilitate strategic reviews, cross-functional planning meetings, and Medical Affairs business reviews.

Cross-functional Collaboration
    • Partner closely with leaders in Field Medical, Medical Communications, Medical Information, HEOR, and Clinical Operations to ensure unified execution and prioritization.
    • Partner closely with leaders across other launch work-streams for aligned strategy and execution
    • Alignment with other launch project management team members to enhance project management effectiveness through collaboration

Operational Infrastructure & Process Excellence
    • Drive the evolution of Medical Affairs operations through process optimization, SOP development, and adoption of best practices.
    • Champion and as needed develop the implementation of medical planning tools

Congress & External Engagement Readiness
    • Lead project management to support operational planning for major scientific congresses, including alignment across abstracts, symposia, and booth activities.
    • Oversee project management supporting coordination and execution of high-impact stakeholder engagements (ad boards, medical education programs, scientific exchange events etc).

Vendor Management:
    • Manage relationships with key vendors and external partners to ensure high-quality, on-time, and on-budget delivery.

Project management:
    • Contribute to developing robust project management tools, processes for launch and day-to-day operations.
    • Partner with other project managers to develop periodic launch management dashboards, meeting materials and actively manage functional, sub-teams and work-streams meetings for effective launch management

The position responsibilities are not limited to the above and might change as the team's needs evolve and includes all other duties as assigned.
Experience, Education and Specialized Knowledge and Skills:
  • Bachelor's (BS) degree required; advanced degree (MS, MBA, PharmD, PhD) or PMP certification preferred.
  • Minimum of 5+ years of experience in project management, operational excellence, reporting, and performance management within biopharmaceutical or life sciences organizations.
  • Minimum of 5+ years of direct project management experience supporting medical affairs
  • Prior experience in pre-commercial or early commercial biotech/pharma strongly preferred.
  • Proven ability to translate complex data into executive-ready insights.
  • Expertise in project management and process improvement methodologies (PMP, Lean, Six Sigma, Agile).
  • Strong analytical mindset
  • Change leadership in fast-paced, evolving environments
  • Proven ability to influence senior stakeholders and drive accountability without direct authority.
  • Willingness to travel 30-50% of the time.

This is the pay for this position
Pay Transparency
$175,000-$200,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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