At MedSource, we believe our employees are just as important as our clients; in fact, they are our best asset. Only by working together can a trial, and a company, be successful.
Our motto, “Taking Relationships as Seriously as Science,” is not simply an empty catchphrase. It’s a standard exemplified by everyone within our clinical research management company. And, we are looking for passionate people to join our team.
Interested in a clinical research career? What You Can Expect from MedSource:
- We are focused, flexible, committed and transparent people who enjoy a work environment that is fast-paced and high-energy.
- Our experienced staff is hardworking, innovative, trustworthy, and full of integrity.
- We understand the need for a proper work-life balance and provide ample flex time and a supportive office culture.
- We hire the most seasoned and experienced team members, from clinical research associates to project managers and data management personnel.
- Each team member is actively involved in our projects from beginning to end, lending them an understanding and appreciation for the whole development process.
If you are interested in furthering your clinical research career at MedSource, please consider our open job positions below.
The Clinical Team Lead is a position of responsibility within a project with the requirement to supervise one or more Clinical Research Associates (CRAs). As a high-profile role within the project, the CTL must be able to interact confidently with the client, maintaining a professional image when working under time constraints and act responsibly as […]
The Administrative Coordinator, Business Development performs a variety of support, research, and administrative duties across the Business Development department. The primary responsibilities are to support the outside Business Development team with research into prospective clients and entry into the CRM system; plan, provide, negotiate, and secure and travel arrangements for industry conferences; and support all […]
Responsible for assisting in the coordination and documentation of activities associated with MedSource budgets and proposals including, but not limited to, change orders, request for proposals, project tracking, task order tracking, and database management. Support budget and proposal development efforts with sponsors, vendors and external suppliers who provide research-related services to the company. Assist leadership […]
The Senior Clinical Research Associate (Sr. CRA) is responsible for interfacing with investigative sites to monitor the conduct and assess the progress of clinical research studies to ensure compliance with protocol(s) and applicable MedSource or Sponsor Standard Operating Procedures (SOPs), FDA regulations, and ICH-GCP guidelines, and any additional applicable regulations as required. With limited supervision, […]
The Clinical Operations Senior Project Manager (SPM) is responsible for overall management of all phases of clinical trials, from start-up through completion of activities, utilizing MedSource or sponsor Standard Operating Procedures (as applicable), FDA regulations, and ICH-GCP guidelines. In-depth knowledge and experience of the drug development process is required, including study initiation, clinical monitoring, drug […]
Supports the management of project-specific Trial Master File (TMF) through the maintenance and filing of clinical records. Provide leadership to junior department and project team members. Assist with development and implementation of training and process improvements. DUTIES AND RESPONSIBILITIES: Perform designated in-house project activities via use of knowledge regarding the application of ICH/GCP guidelines, […]
Lead Clinical Data Manager position is to manage all of data management tasks for multiple studies from study start-up to database lock, to product a clean and analyzable database. Lead Clinical Data Manager is also responsible for the creation of any data collection forms and data validation checks within an electronic data capture (EDC) system […]
The Marketing Manager manages the day to day marketing activities of the organization and develops and implements marketing plans that support the short and long term marketing strategy of the company. The Senior Marketing Manager works with various team members across the organization to align internal and external marketing efforts. DUTIES AND RESPONSIBILITIES: Manage […]
The Training Compliance Specialist works with the Director QA and Manager, QA to develop, manage and coordinate the MedSource training program and is responsible for administering and troubleshooting the Learning Management System (LMS). DUTIES AND RESPONSIBILITIES: Work with Training management to develop and implement training initiatives, assess progress, and focus on the continuous improvement […]
The Director of Business Development is the initial point of contact with potential customers and is responsible for presenting the professional image, capabilities, and competencies of MedSource, Inc. This individual is responsible for driving revenue, territory management, developing new business, retaining and expanding existing business and identifying client needs and sales solutions. Experience in developing […]