Scientist/ Study DirectorScranton, PA, USAReq #4255Tuesday, January 9, 2024Your New Company!At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.About the RoleAre you passionate about advancing preclinical research and making a difference in the field of biopharmaceuticals? If so, we have an exciting opportunity for you to join our team as a Study Director at our cutting-edge Scranton Preclinical site.As the Study Director, you will be the driving force behind the successful execution of assigned studies. From study design to result interpretation and reporting, you'll represent the single point of control, ensuring the utmost accuracy, compliance, and quality in all our GLP and non-GLP studies.What You'll Do Here:Collaborate with Sponsors, Study Directors, and other stakeholders during protocol development to optimize study objectives and design.Take ownership of the technical conduct of studies, analyzing and interpreting data to provide meaningful insights in comprehensive study reports.Coordinate and manage study logistics with clients, sub-contractors, and internal departments to ensure seamless execution.Monitor and communicate study milestones throughout different departments, keeping all relevant parties informed and engaged.Oversee the training and education of study personnel, ensuring their readiness to perform their roles efficiently.Uphold compliance with GLPs, regulations, and guidance's, guaranteeing the highest standards in all aspects of study execution.Implement corrective actions and documentation when unforeseen circumstances arise, safeguarding study quality and integrity.Actively participate in client discussions, providing scientific expertise and addressing inquiries related to the studies.What You'll Need to Succeed:A Master's or Doctoral Degree in a relevant scientific discipline or equivalent qualification. Candidates with a Baccalaureate or equivalent degree and substantial experience will also be considered.One to two years of experience in Toxicology would be a strong asset.Proficiency in using and interpreting appropriate mathematical and statistical methods for scientific data analysis.Strong computer skills, enabling you to navigate complex datasets and utilize various software effectively.Excellent communication skills to articulate scientific data interpretation and conclusions clearly and concisely.Outstanding organizational abilities, enabling you to multitask and thrive in a fast-paced, ever-changing environment.A collaborative spirit and the ability to excel in a team-oriented setting, even under significant time pressure.Proven attention to detail, ensuring accurate and high-quality work consistently.Impressive presentation and facilitation skills, with the ability to engage and captivate diverse audiences.Willingness to undergo Study Director Training and receive training on applicable procedures and SOPs.Dedication to continuous professional development, staying updated with scientific and regulatory advancements.Why Join Us:At our Scranton Preclinical Site, we foster a culture of innovation