Precision for Medicine is hiring a Medical Director/Senior Medical Director - Oncology to join our team. Candidates can work remotely in any of the following locations: Italy, UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia.
Position Summary:
The Medical Director serves as the project physician and provides medical and scientific expertise to project teams. The Medical Director's primary focus of work will be to ensure the accuracy and integrity of the data resulting from the trial, with a concentrated focus on patient safety. This position also participates in the strategic planning and execution of critical development programs for a variety of clients in haematology and oncology, contributes to the development of Precision's Medical team, and supports Business Development activities.
Essential functions of the job include but are not limited to:
Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement. Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings. Write or edit scientific content of deliverables within budget and timelines. Collaborate with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy. Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts). Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports, and new drug applications. Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings, and figures as needed. Serve as a medical resource for study sites, the project team, and clients. Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions. Assume responsibility for medical and safety monitoring on assigned projects. Participate in feasibility discussions relating to specific project proposals. Develop training modules and provide training concentrating on disease states. Participate in process improvement activities. Collaborate with Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally. Qualifications:
Minimum Required: MD, DO, MBBS, or equivalent medical qualifications. 5+ years of clinical experience. 5+ years of experience in oncology clinical research. Board Certification in Oncology. Demonstrated expertise around the lifecycle of oncology drug development with the ability to strategically analyze oncology clinical trial protocols. Availability for domestic and international travel including overnight stays (approximate 30% travel requirement). Preferred: Drug development experience in Oncology. Oncology Fellowship or equivalent. Phase I and Phase II oncology clinical trial experience. Prior CRO experience. Maintains current scientific and medical knowledge base. Skills/Competencies: Ability to deliver on commitments; understands the service culture. Strategic thinker who can build strategic drug development solutions associated with novel development programs, study designs, and patient populations. Demonstrates a high degree of professionalism, as evidenced by punctuality, positive interactions with customers and teammates, including good interpersonal skills. Communicate both verbally and in written form in an acceptable manner. Conduct formal presentations to a wide variety of audiences including colleagues. Strong visual and presentation skills. Ability to work effectively in a fast-paced team setting, with minimal supervision. Proven efficiency in working remotely. Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages-from early development through approval-with embedded experience in oncology and rare disease.
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Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. 2020 Precision Medicine Group, LLC
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
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Position Summary:
The Medical Director serves as the project physician and provides medical and scientific expertise to project teams. The Medical Director's primary focus of work will be to ensure the accuracy and integrity of the data resulting from the trial, with a concentrated focus on patient safety. This position also participates in the strategic planning and execution of critical development programs for a variety of clients in haematology and oncology, contributes to the development of Precision's Medical team, and supports Business Development activities.
Essential functions of the job include but are not limited to:
Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement. Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings. Write or edit scientific content of deliverables within budget and timelines. Collaborate with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy. Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts). Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports, and new drug applications. Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings, and figures as needed. Serve as a medical resource for study sites, the project team, and clients. Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions. Assume responsibility for medical and safety monitoring on assigned projects. Participate in feasibility discussions relating to specific project proposals. Develop training modules and provide training concentrating on disease states. Participate in process improvement activities. Collaborate with Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally. Qualifications:
Minimum Required: MD, DO, MBBS, or equivalent medical qualifications. 5+ years of clinical experience. 5+ years of experience in oncology clinical research. Board Certification in Oncology. Demonstrated expertise around the lifecycle of oncology drug development with the ability to strategically analyze oncology clinical trial protocols. Availability for domestic and international travel including overnight stays (approximate 30% travel requirement). Preferred: Drug development experience in Oncology. Oncology Fellowship or equivalent. Phase I and Phase II oncology clinical trial experience. Prior CRO experience. Maintains current scientific and medical knowledge base. Skills/Competencies: Ability to deliver on commitments; understands the service culture. Strategic thinker who can build strategic drug development solutions associated with novel development programs, study designs, and patient populations. Demonstrates a high degree of professionalism, as evidenced by punctuality, positive interactions with customers and teammates, including good interpersonal skills. Communicate both verbally and in written form in an acceptable manner. Conduct formal presentations to a wide variety of audiences including colleagues. Strong visual and presentation skills. Ability to work effectively in a fast-paced team setting, with minimal supervision. Proven efficiency in working remotely. Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages-from early development through approval-with embedded experience in oncology and rare disease.
#LI-NC1 #LI-Remote
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. 2020 Precision Medicine Group, LLC
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
#J-18808-Ljbffr
