Associate Medical Director Clinical Science
1 settimana fa
- Full-time
- Sobi Location: United States
Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application
At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.
Here at Sobi, our mission and culture get us excited to come to work every day, but here are a few more reasons to join our team:
- Competitive compensation for your work
- Emphasis on work/life balance
- Collaborative and team-oriented environment
- Opportunities for professional growth
- Diversity and Inclusion
- Making a positive impact to help ultra-rare disease patients who are in need of life-saving treatments
Role & Function
The Associate Director Clinical Science is responsible for Sobi’s clinical development activities and serves as scientific and medical expert on matters relating to the assigned development program including regulatory and drug safety.
Key Responsibilities
- Provide clinical, medical, and strategic input to clinical development plans, while adhering to the highest scientific and ethical standards.
- Responsible for planning, designing, conducting (including medical monitoring) and reporting Sobi-sponsored studies, in close collaboration with the Medical Development Lead (MDL), Medical Program Lead (MPL) and clinical study teams, regulatory, safety and other cross-functional HQ teams, as applicable.
- Act as Study Physician responsible for Sobi-sponsored studies.
- Member of the Medicine Development Team and of Clinical Study Team(s).
- Interact and consult with key opinion leaders and lead advisory boards to define the development plan for new products/indications.
- Responsible for the development of clinical study synopsis and protocols, contribute to the statistical analysis plans, participate in Investigator meetings and other study-related activities and provide input/review of other main clinical study documents, as needed and appropriate.
- Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities.
- Contribute with high-quality scientific and medical input to delivery of clinical parts of submissions and other regulatory documents as well as to responses to Health Authority’s questions to support e.g., scientific advice, IND application, marketing authorization.
- Where applicable and assigned, provide scientific and medical expert support to other functions within Sobi on specific therapeutic area of expertise, including global safety, medical affairs activities such as advisory boards, scientific communications & publications, and business development such as due diligence evaluations of external compounds and M&A.
Minimum Requirements
- Medical Degree required.
- At least 3-4 years clinical experience treating patients (rheumatology/immunology preferred) and/or at least 4-5 years of solid record of accomplishment within rheumatology/immunology drug development programs demonstrating outstanding and intimate understanding of various phases of clinical trials.
- Expertise in bringing the medical and scientific perspective, drug development wisdom to business development, corporate strategy and leadership decision making.
- Good communication skills, capable of representing the company to all audiences both internally and externally, particularly in the context of collaborations at international conferences and scientific symposia.
- Good organizational skills, be a self-motivated driver of best practices and processes in the management of projects and operations.
- Good team-player with high personal and scientific integrity.
- Comfortable working in fast paced environment.
- Able to demonstrate behaviors in line with Sobi’s core values: Care, Ambition, Urgency, Ownership and Partnership.
- Ability to work effectively in a matrix, cross-functional setting; excellent collaboration skills; and experience working with co-development/co-commercialization industry partners would be beneficial.
- Able to work well in a virtual environment. Proven self-management by showing initiative, good organization and willingness to be held accountable.
- Proficient level of English.
Why Join Us?
We are a global company with over 1,700 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.
We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.
Sobi Culture
At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them.
As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.
An Equal Opportunity Employer
Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate.
Sobi is an affirmative action and equal opportunity employer. Disabled/Veterans. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to talentacquisition@sobi.com.
#J-18808-Ljbffr-
Associate Medical Director Clinical Science
3 settimane fa
Milan, Italia Sobi A tempo pienoJob DescriptionRole & FunctionThe Associate Director Clinical Science is responsible for Sobi’s clinical development activities and serves as scientific and medical expert on matters relating to the assigned development program including regulatory and drug safety.Key ResponsibilitiesProvide clinical, medical, and strategic input to clinical development...
-
Medical Director, Rheumatology
2 mesi fa
Milan, Italia ICON plc A tempo pienoMedical Director, Rheumatology ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Rheumatologist to join our diverse and...
-
Medical Director- Oncology/Hematology
6 mesi fa
Milan, Italia IQVIA A tempo pienoJob Overview The medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical...
-
Clinical Research Associate
6 mesi fa
Milan, Italia AstraZeneca A tempo pienoAt AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As a Clinical Research Associate (CRA) in Italy, you will play a pivotal role in channelling our scientific...
-
Associate Director, Regulatory Affairs
2 mesi fa
Milan, Italia Cpl Healthcare A tempo pienoJob Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: Italy (Milan) – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to...
-
Associate Director, Regulatory Affairs
2 mesi fa
Milan, Italia Cpl Healthcare A tempo pienoJob Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: Italy (Milan) – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to...
-
Clinical Trial Assistant
1 settimana fa
Milan, Italia Dompé farmaceutici S.p.A. A tempo pienoThe Clinical Trials Assistant (CTA) is responsible for project-supporting clinical drug research and development tasks. The CTA will provide administrative and clinical trials assistance to the Project Managers and project team for start-up, active phase, and closeout activities for assigned clinical studies.ResponsibilitiesTo provide general administrative...
-
Clinical Research Associate II
1 mese fa
Milan, Italia Psi CRO Ag A tempo pienoClinical Research Associate II / Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organization with more than 28 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a...
-
Clinical Research Associate II
3 settimane fa
Milan, Italia Psi CRO Ag A tempo pienoClinical Research Associate II / Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organization with more than 28 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a...
-
Clinical Start up Manager Milan
1 mese fa
Milan, Italia Resourcing Life Science A tempo pienoCompany DescriptionOur client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Start up Manager office based in Milan.Job OverviewLeading cross-functional project...
-
Clinical Research Associate
1 settimana fa
Milan, Italia Thermo Fisher Scientific A tempo pienoWork ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeAt PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to...
-
Sr Director, Medical Strategy Lead
6 mesi fa
Milan, Italia IQVIA A tempo pienoThe IQVIA Cardiovascular Center of Excellence, a hub of clinical innovation, is growing! We are looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular Medical Strategy Lead...
-
Senior Clinical Research Associate
1 mese fa
Milan, Italia ICON Plc A tempo pienoSenior Clinical Research AssociateICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently recruiting for an experienced Sr. CRA - Italy...
-
Sr. Clinical Research Associate
1 mese fa
Milan, Italia ICON A tempo pienoICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently recruiting for an experienced Senior Clinical Research Associate in Italy to work...
-
SC Medical Director
8 mesi fa
Milan, Italia Kyowa Kirin A tempo pienoOverview WE PUSH THE BOUNDARIES OF MEDICINE. LEAPING FORWARD TO MAKE PEOPLE SMILE At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We are an inclusive...
-
Copy of Country Medical Lead, Italy
3 settimane fa
Milan, Italia Guardant Health A tempo pienoJob Description About the Role: Based in Italy, the primary role of the County Medical Lead, Medical Affairs (MA), is to educate and develop academic key opinion leaders (KOL) champions with the most current study findings (abstracts, publications and evidence pipeline) supporting the clinical value of Guardant Health’s products. The Country...
-
Medical Science Liaison Nord Est
7 mesi fa
Milan, Italia Biogen A tempo pienoJob Description The MSL provides field-based medical/scientific expertise ensuring understanding of the disease area and Biogen’s products as appropriate. They are integral to building valued constructive partnerships with key stakeholders in the medical community and the healthcare system. MSLs contribute to company success through both internal and...
-
Senior Clinical Research Associate
7 mesi fa
Milan, Italia Worldwide Clinical Trials A tempo pienoRequisition Number7552Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...
-
Sr. Clinical Research Associate
1 mese fa
Milan, Italia Allucent A tempo pienoAt Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will independently...
-
Sr. Clinical Research Associate
1 settimana fa
Milan, Italia Allucent A tempo pienoAt Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will independently...