Several years' experience in Clinical Research. Excellent understanding of the principles of clinical study management. Good clinical knowledge with an understanding of medical terminology. Previous experience working within phases II / III. Proven leadership experience of integrated teams.
A staffing agency is filling a position for a Telecommute Medical Communications Project Coordinator. Core Responsibilities Include: Maintaining internal databases to ensure successful management. Working directly with clients to make sure objectives are aligned.
A medical device manufacturer is filling a position for a Remote Clinical Trial Project Manager. Core Responsibilities Include: Clinical trial project management, in the medical device field. Managing CROs. Ensuring on time or early study completion/deliverables.
A medical contract research organization is seeking a Remote Regulatory Affairs Manager. Core Responsibilities Include: Preparing, submitting, and managing regulatory clearance applications. Preparing and submitting USFDA Regulatory submissions.
10+ years of experience in clinical/scientific leadership or management role. Master or PhD in a scientific discipline. 5+ years of experience in managing a clinical research functional team. Knowledge and experience with global medical software regulations.
A clinical research organization is seeking a Remote Medical Writing Associate Director. Individual must be able to fulfill the following responsibilities: Implementing document quality controls, standards and best practices.
A staffing company is seeking a Remote Medical Communications Project Manager in Yardley. Candidates will be responsible for the following: Assisting account manager in supervising & keeping projects within budget. Managing the production and delivery of projects.
A staffing company has a current position open for a Remote Medical Communications Project Manager in Morristown. Candidates will be responsible for the following: Developing and managing project timelines, budgets, and client service expectations.
Collaborating with the Medical Writer on clinical regulatory documents. Must meet the following requirements for consideration: 20-30% travel required. BS with 7+ years’; or MS with 5+ years’; or PhD with <2 years’ relevant career experience. Oncology experience required.
Demonstrated extensive data management skills and thorough knowledge of the data management process. Previous experience and shown competence in leading delivery of multiple projects. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.