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 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 point of […]
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 Finance Specialist is responsible for assisting in the coordination and documentation of activities associated with MedSource finance including, but not limited to, invoicing, expense report reviews, project tracking, work order tracking, and database management. This individual will be expected to interact with MedSource staff and clients and will exercise judgment in all communication. Additional […]
Develops domestic and global proposal budget and text documents for strategic and complex proposals and/or rebids. Assists in the supervision and quality control (QC) of the proposal development process and delivery. Mentors and/or trains less experienced staff members. This individual will be expected to interact with staff and clients and will exercise judgment in all […]
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 […]