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 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 […]
Supports clinical operations through administrative support of functional leads to ensure successful completion of project deliverables and effective management of clinical trials. 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 for assigned projects. Serve as […]
An accounts payable analyst has the responsibility to ensure that the reporting, evaluating, and processing of payments’ expense records are done accurately. DUTIES AND RESPONSIBILITIES: Supervise, input, assemble, and review incoming bills and records of expenditure by employees. Handle statements of credit cards to ensure proper documentation prior to fulfillment of payment. Prepare monthly reconciliations […]
The Data Management, Project Manager (DMPM) 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 for data management and may include statistics and medical writing activities. Acting as the primary contact for the customer for all delivery activities, the DMPM […]
The Senior Biostatistician provides statistical input into Phase I – IV clinical trial development. Responsibilities include statistical input into protocol development (e.g., trial design, sample size estimation, randomization, statistical methods for protocols); developing statistical analysis plans (SAPs) and mock tables listing and figures (TLFs), statistical analysis, and writing detailed statistical analysis plans including specifications for […]
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 the overall management of all phases of clinical trials utilizing MedSource or sponsor Standard Operating Procedures (SOPs) as applicable, FDA regulations, and ICH-GCP guidelines. The Senior PM possesses in-depth knowledge of and experience in the drug development process, including study start-up, initiation, clinical monitoring, drug […]