Company

Kumquat Biosciences IncSee more

addressAddressSan Diego, CA
type Form of workFull-Time
CategoryHealthcare

Job description

Job Description

Description:

At Kumquat, we strive to develop life changing medicines in an efficient and innovative way with the shared mission of patient focus. The Medical Director/ Senior Medical Director plays an essential role in leading the development program of a study drug, innovative clinical trial design, execution of clinical studies with the study management team, and medical monitoring to bring better clinical trials to more patients.


We want you to join our mission and be part of our passionate and collaborative community, We value individual and team accountability and also see the potential of all our people to learn, grow, develop and achieve great things beyond the confines of traditional descriptions.


Medical/ Senior Medical Director:

Reporting directly to the CMO

Leading a cross functional team for a study drug from the first in human study all the way to registration by:

Providing clinical and strategic input to senior management.

Overseeing and be accountable for input and execution of the clinical development plan by developing and executing protocols and protocol amendments

Engaging effectively with key thought leaders and investigators

Actively participating in study/ site start-up activities, medical monitoring, data cleaning, data interpretation and provide general clinical support to the study team(s)

Serve as a partner to external stakeholders in various countries and help support local needs.

Maintains up-to-date knowledge on the emerging treatment landscape in study specific areas

Cultivate meaningful peer-to-peer collaborations and nurture a culture of curiosity to enable faster, simpler, and more patient-centric ways of operationalizing our studies.

Work with colleagues across Kumquat to promote communication and community. Optimizing growth opportunities and capabilities to successfully contribute and operate in a diverse and global environment. Drive new thinking by identifying new opportunities and options to embrace value creation.

Ensure GCP/GVP compliance, data integrity, and take a balanced risk-based approach in the work you are focused on, seeking guidance or direction as needed.


Who you are:

You are a talented and passionate human, inspired by our shared purpose to innovate clinical trial delivery to bring better trials to more patients.

You thrive in environments of ambiguity and collaboration where the ability to make sound decisions quickly while seeking advice when needed is essential.

You apply your organizing and problem-solving skills to run efficient teams

You are an effective communicator that shares information transparently and strategically. You are comfortable working out loud and are an active listener.

You thrive leading or being an active member of large or small diverse teams.


Expectations:

Knowledge of Clinical development such as study design, protocol execution and medical monitoring and drug development.

Provides subject matter expertise on activities or through supporting the design and execution of clinical trials and/or enabling projects across geographies.

Contributes to the outcome of one or more clinical trials and/or enabling projects.

Independently and with minimal guidance develops plans to support the design and execution of clinical trials and/or enabling projects.

Understands, applies proficient knowledge of, and ensures adherence to ICH, GCP, and regulatory guidelines within clinical trials or enabling activities.

Participates in identifying vendors, builds relationships with sites and investigators and partners to ensure the execution of clinical trials.

Work closely with Investigator and clinical site staff

Requirements:

MD or MD/PhD with oncology and or hematology expertise

At least 5 years of relevant experience either in the pharmaceutical industry, community setting or academia.

Phase 1 and 2 study trial experience in either solid tumor or hematologic malignancies with a focus on small molecules preferred

Working knowledge of Drug Development and Clinical development activities and deliverables.

Experience in developing leadership skills, mentoring and coaching colleagues with less experience, and provide guidance

Ability to solve complex outcomes; takes a new perspective on existing solutions; exercises judgment based on analyzing multiple sources of information and advice.

Ability to explain complex information to others including senior management in a straightforward manner

Ability to travel up to 20% of the time domestically or internationally

Refer code: 7334382. Kumquat Biosciences Inc - The previous day - 2023-12-21 06:21

Kumquat Biosciences Inc

San Diego, CA
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