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 & Duties- Contribute 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 staff
- Medical monitoring activities including but not limited to: review of medical listings, , review protocol deviations, and need for protocol amendments
- Support presentations at scientific, medical, and regulatory meetings globally
- Support the development and maintenance of relationships with investigators, pharmaceutical partners, vendors, key medical experts KMEs, professional societies, and patient advocacy groups
- Support the provision of activities integral to INDs, NDAs and other regulatory submissions such as authoring of clinical sections of related documents
- Partner with pharmacovigilance to assess the safety profile of compounds
- Maintain 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 stakeholders
- Author manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectives
- Ensure clinical development activities are conducted in accordance with applicable regulations, Good Clinical Practice (GCP), company policies, and ethical standards.
Skills & ExperienceRequired Qualifications
- Medical Doctor (MD), or non-US equivalent of MD
- Ability 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 USD
