Previous experience working within phase III studies within Oncology. 4-5 years' experience as a Clinical Study/Trial Manager. Excellent understanding of the principles of clinical study management. Good clinical knowledge with an understanding of medical terminology.
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 has an open position for a Remote Principal BioPharma Medical Writer. Candidates will be responsible for the following: Leading the composition of all clinical and regulatory deliverables. Reviewing all regulatory/clinical documents composed by outside sources.
Excellent analytical skills, with the ability to process scientific and medical data. Expertise in manipulating and analyzing SAS data. Ability to identify data issues, present problems, and implement solutions. Familiarity with clinical trial design and analysis activities.
A medical solutions company has a current position open for a Remote Trial Optimization Analyst in Titusville. Must be able to: Operationalize technology and analytical initiatives. Track and apply GCDO country, site, and enrollment performance.
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.
Knowledge of regulatory guidelines and directives, and knowledge of medical therapeutic areas. Strong knowledge of the clinical development process required. All other requirements necessary for this position.
A staffing agency is filling a position for a Telecommute Medical Device Clinical Evaluation Reports Writer in Tampa. Core Responsibilities of this position include: Performing all clinical writing from to start to finish.
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.
A biopharmaceutical company is searching for a person to fill their position for a Remote Senior Regional Medical Liaison. Individual must be able to fulfill the following responsibilities: Provide clinical and economic value information to payers.