Senior Scientist/Study Director- RLT
- LE4001 Imanova Limited
- US MA Needham
- 5mo ago
- Full-Time
- On-site
What can we offer you?
Apart from job satisfaction, we can offer you:
HEALTH
Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA)
YOURSELF
Paid time off policy including holidays and sick time
Internal growth and development programs & trainings
WEALTH
401(k) program, life & accident insurance and disability insurance
Key Responsibilities
Scientific Leadership
Responsible for scientific output and program leadership at Scientific Lead level; accountable for managing technical, process, or sponsor-driven escalations from study team
Study Execution
Drive study design, project planning, and quote generation in conjunction with customers and our Commercial Office
Act as the key representative of Perceptive Discovery to sponsors during all phases of study execution
BD Support
Support and help drive key account management efforts in collaboration with our Commercial Office
Study Director
Drive study preparation, oversee execution, analysis, and reporting of pre-clinical studies in role as Study Director, while following department workflows and ensuring collected and reported data meet high-quality standards
Scientific Writing
Author and/or review technical documents, including study design quotes, study and IACUC protocols, final reports, presentations, abstracts/manuscripts/white papers, etc.
Management
Small team of local and/or remote Study Directors may report directly into this role; responsible for training, technical and process mentoring, and performance management
Scientific Mentor/Collaborator
Support and educate teammates in your key areas of scientific expertise
Nurture a collaborative internal team environment
Functional Competencies (Technical knowledge/Skills)
Significant domain knowledge in a technical area related to imaging, biomarker research, or pharmacology (e.g. preclinical PET, SPECT, CT, MRI, optical imaging; efficacy or tolerability studies; biodistribution or pharmacokinetic studies
Hands-on experience acquiring pre-clinical imaging data, familiarity with data acquisition, analysis techniques, quality control, and experience in interpretation and presentation of such data
Preferred:
Expertise in oncology (preclinical model development)
Expertise in small molecule or biologics radiochemistry
Experience with relevant in vitro/ex vivo methodologies including radioligand binding, autoradiography, and immunohistochemistry
Ability to work effectively and efficiently in a team environment and interact professionally with collaborators, customers, and/or subcontractors
Excellent time and project management skills
Ability to demonstrate adaptability, a logical approach to problem-solving, and a commitment to continual learning
Excellent written and verbal communications skills
Strong presentation skills; able to clearly and compellingly present complex scientific results and service capabilities to colleagues internally and externally
Experience, Education, and Certifications
Scientific/technical PhD in a relevant field (e.g., Biology, Biochemistry, Pharmacology, Toxicology, Engineering, Physics, etc.) with 5-10+ years applicable industry experience or equivalent; or, scientific/technical Masters with 7-12 years applicable industry experience or equivalent
Experience with image processing software
Experience with Microsoft office
English: Fluent