- Clinical Site Activation Coordinator
- Senior Director, Talent Acquisition
- Biostatistician/Senior Biostatistician
- Benefits Manager
- Bioinformatics and Computational Scientist
- Medical Editor
- Senior Manager, Regulatory Affairs
- Medical Director/Senior Medical Director, Pharmacovigilance
- Accounts Payable Coordinator
- Senior Director Clinical Pharmacology
- Statistical Programmer
- Medical Writer
- Contracts Manager
- Lead Clinical Data Manager
- Clinical Supply Chain Manager
The Karyopharm Workplace
Karyopharm Therapeutics, Inc. (the "Company") is an equal opportunity employer. All qualified applicants will be considered without regard to age, race, color, sex, religion/creed, national origin, marital status, ancestry, citizenship, military, reservist or veteran status, pregnancy, sexual orientation or preference, gender identity, gender expression, physical or mental disability, genetic predisposition or carrier status, or any other category protected under applicable federal, state or local law. Consistent with its obligations under applicable law, the Company will make reasonable accommodations for qualified individuals with disabilities. If you require an accommodation in the application process, please contact a member of the Company’s Human Resources department.
Position: Medical Director
The Medical Director will serve as the primary medical lead for Karyopharm clinical trials with cross-functional study teams on clinical trial strategy, design and execution. Along with this, the Medical Director will serve as the primary Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials. This individual will work on multiple trials in Phases 1 through 3.
- Participates in the development of Study Protocols, Investigator’s Brochures, Clinical Development Plans and other key study documents in conjunction with other line functions and with minimal guidance.
- Serves on cross-functional teams for assigned trials, working with other team members to achieve efficient, high-quality study execution.
- Participates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of IND’s and CTA’s, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate.
- Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR).
- Acts as liaison between Clinical Development and other internal groups at Karyopharm (e.g., Regulatory Affairs, Clinical Operations, Clinical Data Management) for assigned studies.
- Represents Karyopharm to outside medical personal in the development of clinical protocols and study conduct.
- MD, DO or equivalent ex-US medical degree (non-MD candidates with doctoral degrees may be considered if they have an appropriate background in a clinical field).
- Minimum of 5 years clinical research experience in an academic or industrial setting, with experience in analysis of research data and publications; working knowledge of biostatistics and pharmacokinetics; working knowledge of GCP, scientific and clinical research methods and clinical study design, regulatory requirements for clinical studies;
- Pharmaceutical/Biotech industry experience, including time managing clinical trials and/or clinical development program(s)
- Excellent oral and written communication skills
- Ability to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriate
- Board certification/eligibility in Oncology is highly desired
- Global clinical research experience and experience interacting with regulatory authorities
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