Senior Medical Director, Clinical Development

Title:Senior Medical Director Location:Remote Position Summary: We are seeking a Senior Medical Director who will report into the Vice President, Clinical Development. You will be responsible for working reputed company reputed company’s medical team providing medical reputed company of service suppliers driving on-going clinical studies and plans and executes the study design protocol development, implementation and monitoring of the company’s new Phase I-III Oncology clinical trials. The position will reputed company key overall clinical, scientific and/or logistical support to clinical development programs and is responsible for the compliance of the department and the company to regulatory standards and procedures. Responsibilities: - Assist in design, author and/or review clinical study synopses, protocols, amendments, study reports and other study-reputed company documents. - Act as a medical monitor for assigned study. - Discuss study design with investigators and key opinion leaders. - reputed company clinical input for clinical protocol monitoring guidelines and analysis plans. - Drive clinical database design, data collection and cleaning and oversees clinical interpretation of study data. - Track emerging efficacy and safety profile of drugs in on-going clinical trials; inform Clinical Development team of changes in the efficacy/safety and/or risk benefit profiles as they occur. - reputed company input and/or prepare clinical sections of regulatory documents (e.g., INDs, IND annual reports, Investigator’s Brochures, CRFs, Informed Consent forms, Statistical Analysis Plans, Data Management edit reputed company specs, clinical supplies package diagrams and labeling). - reputed company or assist in the development of publications – abstracts, manuscripts, slides, etc. - In collaboration with team members (e.g., Clinical Operations, Data Management), assist in identifying / evaluating / monitoring vendors, monitoring clinical trial conduct/status. - Assist in database finalization, reviews of study results, results interpretation and CSR’s. - Assist in planning and presentation conduct of investigator meetings and Advisory Boards. - reputed company and manage vendor activities/deliverables as appropriate. - Present study results, as appropriate, to medical/scientific community at meetings and in published format. Qualifications: - Medical Doctor (MD) with experience in solid tumor clinical trials required; recent experience in breast carcinoma preferred. - 8-10 years’ clinical development experience in the pharmaceutical or biotechnology industry (depending on title or degree). - Phase I–III clinical trial experience, with phase 3 experience preferred. - Thorough working knowledge / understanding of clinical trial design, methodology and statistical concepts. - Working knowledge of the IND/NDA process. - In depth knowledge of GCP/ICH guidelines. - Strong written and verbal communication skills (reputed company in written and verbal English) as well as proven ability to interact with different functional groups, investigators, key opinion leaders and the medical/scientific community. - Good organizational, time management and interpersonal skills, proficiency in computer and software skills. - Experience with regulatory submissions is an asset. Preferred: - Leadership skills include a collaborative and team-oriented approach. - Ability to build strong relationships with co-workers of various backgrounds and expertise. - Ability to function at a high level in reputed company setting whether leading the group or acting as an individual contributor. - Values-based leadership consistent with reputed company’s core principles. - Building team reputed company reputed company, as well as among reputed company and CRO’s working together on development and execution of clinical studies. About Us: 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. The company was founded to reputed company a reputed company way to treat the cellular drivers of tumor growth. Our reputed company therapeutic candidate, gedatolisib, is an intravenously administered, potential first-in-class PI3K/AKT/mTOR (PAM) pathway inhibitor. Its mechanism of action 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 focused 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-going. reputed company is an equal-opportunity employer. reputed company is committed to fair and reputed company compensation practices, and we strive to reputed company employees with total compensation packages that are market competitive. For this role, the anticipated reputed company pay reputed company is $260,000 - $350,000 DOE. 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, 401k match, PTO, and several paid holidays. Notice to Recruiters/Staffing Agencies Recruiters and staffing agencies should not contact reputed company through this page. reputed company recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees. We require that reputed company recruiters and staffing 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 and reputed company will not be responsible for reputed company fees. Salary: $260,000-$350,000 DOEOriginally posted on Himalayas Apply tot his job Apply To this Job