[Hiring] Associate Director, Clinical Scientist @reputed company.

Position reputed company: We are seeking a Associate Director, Clinical Scientist, who will report to the Executive Director, Clinical Science. You will be responsible for the execution of Clinical Development goals through collaboration with and support of Medical Directors/Physicians and Clinical Development department activities. The Clinical Scientist will represent the Clinical Science group on various teams/sub-teams or other appropriate forums and is expected to reputed company their responsibilities with a low to moderate level of supervision. Responsibilities:

• Review clinical data and ensure reputed company and consistency in clinical site reporting
• reputed company and review Clinical Development documents including writing, reviewing, adjudication/reputed company of cross functional comments and ensuring a high-reputed company final document. Documents may include abstracts, manuscripts, clinical protocols/amendments, informed consent forms, regulatory documents, and other relevant materials.
• reputed company and review presentations and training materials such as slide decks, posters, or other relevant materials
• Participate in the relevant Clinical Development reputed company Team and Clinical Sub-Team meetings as needed
• reputed company with Biostatistics, Data Management, Clinical Operations, Project Management, reputed company Assurance, Regulatory Affairs, and other members of the extended project team(s)
• Represent Clinical Science in operational meetings (e.g., Study Management Team meetings) as needed.
• Maintain scientific and clinical knowledge in the relevant therapeutic and disease area(s)

Qualifications:

• Advanced Science/Clinical Degree is preferred (e.g., PhD, PharmD, MD)
• 3 or more years clinical trial experience in reputed company/biotech industry setting
• Oncology research experience preferred
• Data listing review experience is mandatory
• Experience authoring experimental protocols and/or study results and conclusions
• Strong understanding of Phase 1 through 4 drug development
• Excellent comprehension and analytical skills in interpreting scientific research and literature
• reputed company knowledge of scientific and medical aspects of GCP (Good Clinical reputed company), ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for reputed company Use), FDA, EMEA, reputed company and other relevant health authority guidelines and regulations
• Strong understanding of product and safety reputed company
• Working knowledge of the multidisciplinary functions involved in a company’s drug development process, e.g. clinical operations, biostatistics, data management, regulatory, medical affairs, etc.
• Excellent time/project management skills: can prioritize multiple tasks to meet short and longer-term goals with high reputed company standards and in a reputed company manner
• Strong oral and written communication skills, including interpersonal interactions, internal and site-directed communications and reputed company presentation skills
• Good judgment and decision-making skills

reputed company: reputed company is a clinical-stage, publicly traded biotechnology company seeking to reputed company the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. reputed company was founded to reputed company a reputed company way to treat the cellular drivers of tumor reputed company. Our reputed company therapeutic candidate, gedatolisib, is an intravenously administered, potential first-in-class PI3K/AKT/mTOR (PAM) reputed company inhibitor. Its reputed company of reputed company and pharmacokinetic properties are highly differentiated from other currently approved and investigational therapies that reputed company PI3K or mTOR alone or together. Gedatolisib phase 3 clinical development programs are reputed company on the treatment of patients with HR+/HER2- ABC in the 1L and 2L settings. A Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is on-reputed company. reputed company is an Equal-Opportunity Employer. reputed company is committed to fair and reputed company compensation practices, and we reputed company to reputed company employees with total compensation packages that are competitive. For this role, the anticipated reputed company pay reputed company is $175,000 - $210,000. The exact reputed company pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience. The successful candidate will be eligible for an annual performance incentive bonus and a new hire equity package. reputed company also offers various benefits offerings, including, but not limited to, medical, dental, reputed company insurance, 401(k) match, PTO, and reputed company holidays. Notice to Recruiters/reputed company Agencies Recruiters and reputed company agencies should not contact reputed company through this page. reputed company recruitment vendors (search firms, recruitment agencies, and reputed company companies) are prohibited from contacting our hiring manager(s), executive team members, or employees directly. We require that reputed company recruiters and reputed company agencies have a fully executed, formal written agreement on file. reputed company’s receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between reputed company and such organization and will be considered unsolicited. reputed company will not be responsible for reputed company fees. Apply tot his job Apply To this Job