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 Project Manager (PM) has overall responsibility for the successful planning, execution, monitoring, control and closure of multiple projects. These projects will be managed from initiation to close-out and will cover data management, statistics and medical writing. Acting as the primary contact for the customer for all delivery activities, the PM is also responsible for […]
The CRA Line Manager supervises the Clinical Research Associates (CRAs) and provides oversight to ensure successful monitoring of projects at MedSource. The CRA Line Manager participates in the interviewing and hiring process, recommends monitoring staffing solutions, and manages the performance, training, and growth opportunities of the CRAs. DUTIES AND RESPONSIBILITIES: Serve as main […]
Supports clinical operations through administrative support of functional leads to ensure successful completion of project deliverables and effective management of clinical trials. Provide leadership to junior department and project team members. DUTIES AND RESPONSIBILITIES: Perform designated in-house project activities via use of knowledge regarding the application of ICH/GCP guidelines, applicable regulatory requirements, Standard Operating […]
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. DUTIES AND RESPONSIBILITIES: Perform designated in-house project activities via use of knowledge regarding the application of ICH/GCP guidelines, applicable regulatory requirements, Standard Operating Procedures (SOP), and study-specific requirements […]
The Office Administrator performs a variety of office support and administrative duties across all departments by performing the following duties. DUTIES AND RESPONSIBILITIES: Greets and logs in visitors as appropriate; resolves routine administrative problems and answers inquiries concerning office activities and operations; accepts, screens, and routes telephone calls; maintains log of inquiries as required […]
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 […]
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 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 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 […]