Associate Medical Director

Clinical Development Associate Medical DirectorNearly 37 million Americans are currently affected by Chronic Kidney Disease. At Akebia we take that number very seriously and every day we come to work, with the purpose of bettering the lives of each person impacted by kidney disease and the renal community that serves them. Our tenacious, passionate employees' challenge the status quo and work to develop unique therapeutics that have the potential to set new standards of care for people living with kidney disease. This is life-changing work, and we are all in, are you? Please note that our offices have recently relocated to Waltham, MA. We follow a flexible, "magnet not mandate" approach to in-office work, encouraging in-person collaboration and onsite engagement while supporting hybrid flexibility based on role and business needs.Job Summary:The Clinical Development department is responsible for the medical aspects of development activities, including clinical development plans (CDP) and clinical trials. The Associate Medical Director will contribute to the direction, planning, execution and medical oversight of clinical trials and aligned research activities for one or more clinical development programs. Additionally, he/she will be involved to a varying degree in the analysis and interpretation of data outputs. He/she participates in cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy.Essential Functions & DutiesContribute to the development and execution of clinical development strategies and plans in alignment with program objectives.Impact the development, review, and implementation of clinical trial protocols and related study documents.Collaborate with Clinical Operations and study teams to support successful study execution and address medical and scientific issues that arise during clinical trials.Support and add to the oversight of project-related education of investigators, study site personnel, and study staffMedical monitoring activities including but not limited to: review of medical listings, review protocol deviations, and need for protocol amendmentsSupport presentations at scientific, medical, and regulatory meetings globallySupport the development and maintenance of relationships with investigators, pharmaceutical partners, vendors, key medical experts KMEs, professional societies, and patient advocacy groupsSupport the provision of activities integral to INDs, NDAs and other regulatory submissions such as authoring of clinical sections of related documentsPartner with pharmacovigilance to assess the safety profile of compoundsMaintain a high level of clinical and scientific expertise in the disease area(s) by reviewing the literature, attending medical/scientific meetings, and through personal interchanges with consultants, KMEs, investigators and internal stakeholdersAuthor manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectivesEnsure clinical development activities are conducted in accordance with applicable regulations, Good Clinical Practice (GCP), company policies, and ethical standards.Skills & ExperienceRequired QualificationsMedical Doctor (MD), or non-US equivalent of MDAbility to critically evaluate and interpret clinical and scientific data.Strong written and verbal communication skills.Ability to work effectively in a cross-functional, collaborative environment.Strong organizational skills and ability to manage multiple priorities in a dynamic environment.Base Compensation for this role will depend on a number of factors including a candidate's qualifications, skills, competencies, and experience, and may fall outside of the range shown. Base pay is only one component of the company's total rewards package, all regular employees are also eligible for the corporate bonus program or the incentive compensation program (if applicable), as well as equity. Additional benefits include health care, vision, dental, retirement, PTO, etc.Targeted Base Salary $220,074 —$271,856 USDAkebia is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.