In Vivo PK/PD Research Coordinator (Contract)

Pfizer; Groton (CT); On-site; USD 69,000 - 76,000; Full time

Job summary

Pfizer External Research Solutions (ERS) in Groton, CT is seeking an experienced scientist to support external sourcing workflows for in vivo PK, PD, and PK/PD studies across Pfizer’s drug discovery portfolio. This is a full-time contractor role coordinated between Pfizer project teams, SME, and CROs.

The role requires strong scientific judgment, effective communication across multiple stakeholders, and the ability to prioritize amid evolving information in a matrix environment.

Qualifications

• Bachelor’s degree in a relevant scientific discipline with 10+ years of industry experience, Master’s degree with 5+ or PhD with 1-3+ years of industry experience.
• Demonstrated expertise in vivo PK, PD, PK/PD, and preclinical drug discovery.
• Small molecule, peptide, and/or large molecule PK experience is preferred.
• Experience with reagent provision and/or in vitro biology workflows is highly beneficial.
• Experience working with CROs/Academia-industry partnerships and cross-functional scientific teams.
• Ability to influence without direct authority and operate independently with limited day-to-day direction.
• Excellent written and verbal communication skills, including the ability to translate complex data into practical recommendations.
• Proven ability to manage ambiguity, changing priorities, and multiple assignments in a highly matrixed environment.
• Highly engaged to ensure timely support and able to work with minimum supervision in a short period of time.
• Take ownership of assigned activities, maintain clear documentation, and deliver high-quality work within agreed timelines.
• Ability to work with cross-matrix teams and receive feedback.
• Escalate scientific, quality, or timeline risks promptly and constructively.
• Build effective working relationships quickly and operate as a responsive, solution-oriented service partner.

Responsibilities

• Coordinate external in vivo PK, PD, and PK/PD studies at CROs.
• Ensure compliance with external PK workflow and study requirements as outlined in SOPs.
• Understand and work with internal stakeholders and external CRO to participate in devising study approach, dose selection, sampling strategy, endpoints, bioanalytical requirements, and data interpretation.
• Facilitate externally conducted studies by aligning internal teams and CRO partners on objectives, deliverables, timelines, and scientific expectations.
• Review proposals, protocols, data packages, reports, and execute studies in a timely manner.
• Identify risks and knowledge gaps, resolve barriers, and recommend practical paths forward.
• Support multiple programs while maintaining scientific rigor, responsiveness, accountability, and clear communication.
• Track requests, manage workflow, operations and logistics including tracking of KPIs to ensure timely completion.

Skills

In vivo PK/PD

Cross-functional teams

Scientific communication

Ambiguity management

Independent work

Documentation

Study design

Risk assessment

Project coordination

Education

Bachelor's degree + 10+ yrs

Master's degree + 5+ yrs

PhD + 1-3 yrs

Job description

Pfizer External Research Solutions (ERS) in Groton, CT is seeking an experienced scientist to support external sourcing workflows for in vivo PK, PD, and PK/PD studies across Pfizer’s drug discovery portfolio. This is a full-time contractor role coordinated between Pfizer project teams, SME, and CROs.

The role requires strong scientific judgment, effective communication across multiple stakeholders, and the ability to prioritize amid evolving information in a matrix environment.