Pharmaceutical Project Manager:
Arete Technologies Inc.

Arete Technologies Inc.
Somerville Massachusetts


Clinical Project Manager/Coordinator

• The Clinical Project Manager/Coordinator will be responsible for the project management and coordination of post-market clinical research activities of various devices as well as the coordination between Clinical Research and other stakeholders as needed.

Job Requirements:

Responsibilities include:

• Collaborates with business leads to build and execute well-structured program and project plans, specifically related to development of Post Market Clinical Follow Up Plans and Reports.

• Builds and maintains Microsoft SharePoint sites and other platforms to facilitate effective team collaboration and execution of projects.

• Assists internal project owners and teams on an on-going basis to review and communicate project requests, assess project scope, facilitate project prioritization, report status and deliverables.

• Provide continuous strategic communication designed to update different key stakeholders and senior management on the status of metrics (e.g. key initiatives, cross-functional prioritization and synchronization of initiatives).

• Collaborates with project owners, monitors efforts, assembles key project deliverables and identifies issues and risks requiring escalation when reporting project status.

• Schedules and facilitates project status meetings and advises management on project status, including executive reporting as needed.

• Facilitates problem resolution with support from business leads as needed.

• Communicates project implementation options, schedule, quality and risk to stakeholders as well as offer recommendation based on these elements.


• A Bachelor's degree in Biological Science or related discipline, with a minimum of 4 years project management or project coordination experience is required.

• Demonstrated experience in developing / supporting execution of project plans within is required.

• Experience with SharePoint and Microsoft Project is required, with experience in other software desirable.

• Previous experience in the medical device or other regulated industry is required.

• Ability to communicate effectively and work with teams in a matrix environment is required.

• Clinical research experience is strongly preferred.

Will this position require the handling of a controlled substance?


Basic Qualifications