Lead regulatory strategy for Worldwide Clinical Trials across Europe and Canada, shaping proposals, bid defenses, and customer deliverables globally.

Apply Regulatory

Affairs expertise and global startup knowledge in a leadership role.

As Director, Regulatory Pre-Award Strategy, you will direct business development and pre-award activities for competitive proposal offerings. You will design regulatory strategies, oversee proposal development, approve deliverables, and build department-wide training. The role connects Regulatory, Business Development, Therapeutic Area, Project Management, and Site Management functions.

Key Responsibilities

Direct pre-award regulatory strategies and customer deliverables

Lead bid defense meetings and presentations

Develop comprehensive pre-award site activation strategies





Implement department-wide training and coaching programs

Coordinate resource projections and staffing forecasts

Requirements

Minimum twelve years global clinical pharmaceutical industry experience

At least three years managing global teams

Solid Regulatory Affairs experience in Pharma, CMC, or Preclinical

University degree or related allied health certification

Fluent English and local office language; valid passport

Use global Regulatory Affairs expertise, proposal leadership, and coaching skills to advance Worldwide Clinical Trials pre-award strategy.

📌 Regulatory Pre-Award Strategy Director (Winnipeg)
🏢 Worldwide Clinical Trials
📍 Winnipeg