Senior Medical Director, Clinical Development at Celcuity

Minneapolis, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Mar, 26

Salary

350000.0

Posted On

03 Dec, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Oversight, Clinical Trials, Study Design, Regulatory Compliance, GCP Guidelines, Statistical Concepts, Clinical Protocols, Data Management, Vendor Management, Communication Skills, Leadership Skills, Team Collaboration, Solid Tumor Experience, Oncology, Clinical Development, Breast Carcinoma

Industry

Biotechnology

Description

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 within Celcuity’s medical team providing medical oversight 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 provide 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-related documents. Act as a medical monitor for assigned study. Discuss study design with investigators and key opinion leaders. Provide 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. Provide 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 check specs, clinical supplies package diagrams and labeling). Lead 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. Oversee 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 (fluency 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 a team setting whether leading the group or acting as an individual contributor. Values-based leadership consistent with Celcuity’s core principles. Building team within Celcuity, as well as among Celcuity and CRO’s working together on development and execution of clinical studies. About Us: Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth. Our lead 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 target 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. Celcuity is an equal-opportunity employer. Celcuity is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $260,000 - $350,000 DOE. The exact base 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. Celcuity also offers various benefits offerings, including, but not limited to, medical, dental, vision insurance, 401k match, PTO, and several paid holidays. Notice to Recruiters/Staffing Agencies Recruiters and staffing agencies should not contact Celcuity through this page. All 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 all recruiters and staffing agencies have a fully executed, formal written agreement on file. Celcuity’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 Celcuity and such organization and will be considered unsolicited and Celcuity will not be responsible for related fees.

Responsibilities

The Senior Medical Director will provide medical oversight for ongoing clinical studies and execute study design protocol development. They will also ensure compliance with regulatory standards and support clinical development programs.