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Premier Research International

Contract research organization for clinical development

Vice President, Clinical Pharmacology - Clinical Pharmacology

Full-Time
No salary listed
Expert
PharmD, PhD
Remote in USA
RemoteTravel of 10–15%, including inter-office travel, is required.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A Ph.D. in pharmacology, pharmaceutical sciences, PharmD, or a related discipline is required.
  • 10–15 years of experience in clinical pharmacology studies and programs for biological and small molecules, and development of compounds and biologics in a contract research organization, pharmaceutical, biotechnology, or related environment is required.
  • Demonstrated knowledge of the research process and direct research experience are required.
  • Demonstrated scientific writing and editing skills are required.
  • Ability to work collaboratively in a team environment, including with global companies and sponsors, is required.
  • Ability to read, analyze, and interpret common scientific and technical journals is required.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions is required.
  • Ability to effectively communicate technical concepts within a project team in both written and spoken English is required.
  • Flexibility regarding schedule and work projects is required.
  • Ability to travel 10–15%, including inter-office travel, is required.
Responsibilities
  • Provide strategic and operational leadership for the clinical pharmacology team, including planning, budgeting, recruiting, and leading the team.
  • Oversee the design, delivery, and scope of integrated or stand-alone clinical pharmacology services for current and prospective clients, including associated budgets and proposal templates.
  • Lead organizational design and development to cultivate the knowledge and skills needed for effective service delivery, including development of a contractor network.
  • Monitor industry trends and developments to ensure readiness of the clinical pharmacology organization and services to meet client needs.
  • Develop and implement plans and objectives to drive revenue and gross margin growth in alignment with corporate strategy, plans, and goals.
  • Ensure effective working relationships between the clinical pharmacology group and other consulting and clinical development services functions.
  • Support team members in developing and executing client services and directly support clients through billable consulting project work as needed.
  • Interact with the Food and Drug Administration and other regulatory health authorities during drug development meetings, including Pre-IND, EOP2, and Pre-NDA meetings.
  • Prepare and mentor scientists, regulatory professionals, and sponsors for Food and Drug Administration meetings.
  • Oversee or complete data review, protocol design, regulatory submission section authoring and review, including Common Technical Document sections for INDs, BLAs, and NDAs.
  • Monitor operational performance of the clinical pharmacology organization, including individual and team utilization and service delivery effectiveness.
  • Manage assignment of clinical pharmacology team members to business development activities and contracted clients and projects based on capacity and expertise.
  • Represent Premier in the scientific community and marketplace.
  • Support commercial planning and activities and participate as a subject matter expert in business development.
  • Contribute to thought leadership through content development and delivery and attend industry conferences and events.
  • Provide strategic input to the Consulting Leadership Team, including business plans and targets, operational standards, and company culture initiatives.
Desired Qualifications
  • Knowledge of 505(b)(2) programs and regulatory requirements for biologics, gene therapy, and/or vaccines is highly desired.
  • Board certification in Clinical Pharmacology, such as DABPC (AP), is highly desired.

About the company

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Premier Research International

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Premier Research provides specialized clinical development services for biotech and specialty pharma, focusing on specific therapeutic areas where science is advancing. It supports end-to-end clinical trials, including study design, site management, data handling, statistics, regulatory affairs, and medical writing, across more than 20 countries with about 1,500 employees. Customers partner with Premier Research to plan and run development programs with cross-functional teams that design trials, manage sites and data, analyze results, and prepare regulatory submissions. The company aims to help biotech and pharma bring safe, effective therapies to patients faster by delivering high-quality clinical development and regulatory support.

Company Size

1,001-5,000

Company Stage

Acquired

Total Funding

$79.2M

Headquarters

Morrisville, North Carolina

Founded

1989

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Simplify's Take

What believers are saying

  • Premier extended Daré Bioscience exclusivity in 2026 for U.S. reproductive-health CRO services.
  • Its January 2024 BioCentriq partnership targets faster pre-IND cell therapy timelines.
  • ASCO 2026 highlighted Premier Applied Sciences' myeloma study with Mango Sciences, strengthening credibility.

What critics are saying

  • Indeed rated Premier Research 2.6/5 for job security and advancement in May 2026.
  • Glassdoor reviews cite weak training, overtime, and low trust in upper management.
  • Frequent executive turnover since 2024 signals integration strain if sponsor growth stalls in 2026-2027.

What makes Premier Research International unique

  • Premier Research specializes in biotech, specialty pharma, and medtech, not broad-market CRO work.
  • Its 2026 leadership hires target commercial scale and operational quality, including Paul Spreen and Siân Smethurst.
  • Premier combines clinical execution with regulatory strategy and product development across 20-plus countries.

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Benefits

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

16%
PR Newswire
Apr 7th, 2026
Premier Research appoints Paul Spreen as chief commercial officer

Premier Research, a global clinical research and product development company, has appointed Paul Spreen as Chief Commercial Officer. Spreen brings over 25 years of life sciences leadership experience and will oversee global commercial strategy, business development, marketing and proposals. Spreen previously served as EVP and Chief Commercial Officer at IQVIA (formerly Quintiles), where he held several global leadership positions. His experience spans the full drug development lifecycle, from early discovery through commercialisation, with a focus on scaling organisations during periods of rapid growth and M&A. In his new role, Spreen will drive sustainable growth, strengthen customer engagement and advance Premier's position across the drug development spectrum. The Morrisville, North Carolina-based company specialises in clinical trials and regulatory strategy for the biotechnology sector.

PharmiWeb
Apr 2nd, 2025
Premier Research Expands Clinical Leadership Team With Addition Of Milena Kanova-Petrova, Md, Global Head Of General Medicine

MORRISVILLE, NC, April 1, 2024 – Premier Research is pleased to announce the addition of Dr. Milena Kanova-Petrova as Senior Vice President, Global Head of General Medicine. In this role, Dr. Kanova-Petrova will oversee strategic planning and project execution for all general medicine clinical operations inclusive of internal medicine, women’s health and dermatology.“Our customers are breaking barriers and forging new pathways every day in the pursuit of bettering patient care. The work is complex and specialized, and adding Dr. Kanova-Petrova to our Clinical Leadership Team expands the specialization that we can provide to our customers,” said Premier Research Chief Operating Officer, Michael Arlotto, Ph.D

Labiotech
Jun 13th, 2024
From Ai To Telemedicine: Transforming Clinical Trial Recruitment In 2024

Recruitment is essential for generating data on drug efficacy, which is crucial for the approval of new medical treatments. Clinical trial success hinges on the ability to recruit a sufficient and appropriate number of participants. As Cara Brant, chief executive officer (CEO) of Clinical Trial Media puts it, “Trials are intended to generate data on how a drug works and you can’t generate that data if you don’t have participants in the study. This makes recruitment one of the linchpins of clinical research and drug development as a whole.”However, the landscape of clinical trial recruitment is becoming increasingly competitive. With over 450,000 clinical trials in progress globally, according to Brant. The task of recruiting participants has never been more challenging​​

TrialHub
Jan 31st, 2024
Shaping Patient-Centric Healthcare: Premier Research Collaborates with FindMeCure's TrialHub to Educate Patients About Clinical Research

TrialHub, a leading platform for patient feasibility in clinical trials, is proud to announce its collaboration with Premier Research.

PR Newswire
Jan 8th, 2024
Premier Research And Biocentriq Enter A Strategic Partnership To Accelerate Pre-Ind Timelines And Clinical Translation Of Innovative Cell Therapies

MORRISVILLE, N.C. and NEWARK, N.J., Jan. 8, 2024 /PRNewswire/ -- Premier Research, a preeminent global clinical research, product development, and consulting company, and BioCentriq, a renowned Contract Development and Manufacturing Organization (CDMO), have entered a strategic partnership to revolutionize the pre-Investigational New Drug (IND) process and accelerate the clinical translation of novel cell therapy products.Premier Research/BioCentriq LogoBy leveraging Premier Research's expertise in cell therapy product development and BioCentriq's proficiency in developing and manufacturing and testing cell therapies, the partnership will streamline the process of bringing new products to patients. As partners, Premier and BioCentriq are well positioned to support sponsors seeking to expedite the transition of their innovative cell therapy candidates from research to clinical trials."Partnering with BioCentriq aligns with our commitment to expediting the development of transformative cell therapies," stated Kenneth Ndugga-Kabuye, MD, FACMG, Vice President, Cell and Gene Therapy at Premier Research. "By merging our comprehensive product development expertise with BioCentriq's specialized capabilities we will help sponsors simplify the development process from pre-IND through approval, ultimately accelerating the delivery of innovative therapies to patients in need."This collaboration will harness Premier Research's comprehensive understanding of regulatory requirements, clinical trial design and study execution, alongside BioCentriq's specialized capabilities in cell therapy development."Cell therapy development is extremely complex," added Olu Aloba, PhD, Vice President, Chemical Manufacturing and Control (CMC) Services, Premier Consulting, a business unit of Premier Research, "Nonclinical and Clinical development, CMC, and the CDMO have to work hand in hand to address the scientific, logistical and regulatory demands that enable studies to generate high-quality results.""This collaboration marks a significant step in fostering a more streamlined pathway for groundbreaking cell therapies," remarked Alex Klarer, Vice President, Business Strategy and Innovation at BioCentriq. "Combining Premier Research's clinical insights with our CDMO expertise will empower us to expedite the translation of novel therapies from the lab to clinical reality, benefiting patients worldwide."About Premier ResearchPremier Research, a global clinical research, product development, and consulting company, is dedicated to helping biotech, specialty pharma, and medtech innovators transform life-changing ideas and breakthrough science into new medical treatments.Premier Research specializes in the use of innovative technologies for smart study design and trial management to deliver clean, conclusive data to sponsors.Whether it's developing product lifecycle strategies, reducing clinical development cycle timelines, securing access to patients, navigating global regulations, maximizing the impact of limited rare disease data, or providing expertise in specific therapeutic areas, Premier Research is committed to helping its customers answer the unmet needs of patients across a broad range of medical conditions