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 Senior Validation Engineer will liaise with IT Management and Quality Assurance to execute the Company’s overall computer system validation testing strategy by assisting in the development and coordination of computer systems validation activities. The Senior Validation Engineer will provide direction to ensure that regulated IT applications and infrastructure components possess the necessary level of […]
The Director, BDS manages the Data Management and Biostatistics staff to ensure successful execution of data management and statistical activities as contracted for projects at MedSource. Drives strategy and execution of improving and refining the department infrastructure, expanding in-house (and outsourced) services offerings and technology, process improvement, and quality execution services. Develops or refines resource […]
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 Principal Biostatistician provides statistical input into Phase I – IV clinical trial development, performs the analysis of clinical trial data, and provides statistical input into the reporting of clinical trial results. Responsibilities include: providing statistical input into protocol and case report form (CRF) development in all therapeutic areas (e.g., trial design, sample size estimation, […]
Data Manager is responsible for managing data cleaning tasks, medical coding and vendor data reconciliation. Data Manager will maintain these tasks across multiple studies and EDC platforms. DUTIES AND RESPONSIBILITIES: Be responsible for participating in all data management activities from initiation of protocol through database lock Data Cleaning activities Have the ability to support […]
Lead Data Manager is responsible for managing multiple data management tasks on multiple studies. Lead Data Manager is also responsible for the creation of any data collection forms and data validation checks within an electronic data capture (EDC) system for the purpose of conducting clinical trials. Lead Data Manager is also responsible for Medical Coding, […]
The role of the Senior Revenue Recognition Analyst is to improve the understanding of revenue recognition in the business, including identifying losses, missed areas of revenue, and provide support to Clinical Project Managers, Budgets and Proposals, and Finance in identifying trends in forecasted revenue to actual revenue. DUTIES AND RESPONSIBILITIES: Prepare, reconcile, analyze and report […]
The Manager, QA is responsible for assisting in the development, coordination, and implementation of Good Clinical Practice (GCP) related quality assurance activities. These responsibilities include supporting the development, execution and maintenance of risk based audit programs focused on internal and external GCP audits to ensure that clinical trials are conducted in compliance with applicable regulations, […]
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 […]
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 […]