Associate Protocol Manager

About Bristol-Myers Squibb

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are a passionate industry leading organization committed to making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents, ideas, and integrity to collaborate and swiftly deliver operational excellence and high-quality data. We are driven to make a difference, from cutting edge research, to hands-on community support. Bristol-Myers Squibb recognizes the importance of balance and flexibility, and values diversity and inclusion in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees opportunities for growth, both at work and in their personal lives.

Responsibilities

The Associate Protocol Manager (PTM) is a diverse and challenging role within Global Clinical Operations working in a dynamic matrix project team.

The Associate PTM supports the successful and timely execution of in-house or outsourced clinical research protocols from study start-up to final clinical study report within established budget and timelines.

The Associate PTM works in collaboration with the primary Protocol Manager to monitor protocol progress, address and manage obstacles, and help coordinate the development of protocol level documents and plans.

The Associate PTM can effectively identify issues and risks, and escalates promptly within the protocol team.

The Associate PTM must leverage her/his strong interpersonal and influencing skills to foster partnerships across assigned projects and multidisciplinary teams.

Requirements

A minimum of a BA or BS Degree with 2 to 4 years of demonstrated project management experience of which at least 1 should have been gained in the pharmaceutical or healthcare industry.

Experience working with CROs is a plus.

This candidate should have experience in the execution of clinical research trials management demonstrating strong project management and organizational skills.