Medical Director, Medical Affairs (Lifecycle Management)
Listed compensation
$270k-$305k
Listing transparency3 of 6 stated
Ask the employer about call expectations, weekend coverage and nights and shift pattern.
- Employment & setting
- Full-Time · remote
- Call expectations
- Not specified
- Weekends
- Not specified
Job Description
This is a high impact position with great visibility, and collaboration, across
multiple departments and all levels of the Alkermes organization. This position
will have critical responsibilities in the medical affairs group involved in the
development of therapies for neurology and neuropsychiatric indications across
late-stage programs, contributing to Alkermes’ LCM efforts in neuroscience.
Responsibilities
* Responsible for protocol design and execution across late-stage clinical
research trials in neurologic disorders
* Serve as the LCM Lead for multiple programs, including leadership of the
subteams of those programs
* Direct authorship contributions in protocols, clinical study reports, study
documents, regulatory documents, and external publications
* Provide medical oversight of clinical trial data and medical monitoring (in
conjunction with a CRO medical monitoring team) of clinical trials supporting
sNDA indications and LCM studies
* Critically review and contribute to regulatory interactions for LCM studies,
sNDAs
* Develop LCM plans with cross functional teams and contribute to strategic
discussions related to LCM plans and indications
* Develop strategy for Investigator Sponsored Studies (ISS) program with cross
functional team members and serve on the ISS review committee as a reviewer
* Responsible for strategy and execution of product specific global expanded
access and compassionate use programs in collaboration with the EAP team
* Represent the company to external audiences, including clinical sites, key
opinion leaders, and patient advocacy groups
* In collaboration with clinical operations, oversee and coordinate the
operational aspects of ongoing projects to ensure that goals of time, cost
and quality performance expectation are met
* Ensure that standard operating procedures (SOP) for the LCM team facilitate
the development of effective clinical research programs and are compliant
with clinical/medical and industry standards
* Identify and develop collaborative relationships with key investigators, and
key thought leaders globally. Attend, plan, and oversee life cycle management
clinical advisory boards and investigator meetings, and present at major
medical conferences
Qualifications
* MD with experience in Neurology or Psychiatry required
* Board Certification in Neurology or Psychiatry preferred
* A minimum of 2+ years of experience in the pharmaceutical industry in medical
affairs/ clinical development or LCM functions
* A business-focused individual, with experience in all aspects of drug
development across late-stage clinical programs
* Experience interacting with global regulatory agencies, including successful
sNDA submissions, label expansions and approvals is highly desired
* Outstanding written and verbal communication, with experience interacting
with and presenting to senior management and external audiences
* Ability to navigate complexity and ambiguity in a highly matrixed work
environment
* Demonstrated leadership and collaborative interpersonal skills, fostering
teamwork and cross-functional partnerships
* Self-motivated with the ability to work independently, prioritize tasks
efficiently, and meet deadlines
* Detail-oriented with expertise in conducting thorough and timely reviews of
medical and trial related documents
Alkermes has recently adopted a hybrid working environment to support and meet
the needs of employees and this role will operate in a flexible environment with
60% of time in the office and 40% from home. This position is eligible for the
hybrid workplace model, requiring work to be completed onsite at our Waltham, MA
office at least 3 days per week. This role is not eligible for fully remote
work.
The annual base salary for this position ranges from $270,000 to $305,000. In
addition, this position is eligible for an annual performance pay bonus. Exact
compensation may vary based on skills, training, knowledge, and experience.
Alkermes offers a competitive benefits package. Additional details can be found
on our careers website: www.alkermes.com/careers#working-here
[http://www.alkermes.com/careers]
#LI-MB1
Qualifications
- Education
- Doctoral or professional degree (postgraduate degree)
Certifications
Key Skills
Work-Life Balance Analysis
WeekdayDoc's proprietary algorithm rates Medical Director, Medical Affairs (Lifecycle Management) at Alkermes a 6.1 out of 10 for work-life balance — classified as good. This places the position in the Above average in Medical Affairs — ranked against 193 active Medical Affairs listings on WeekdayDoc. Contributing factors include remote work flexibility.
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