Overview
Senior Principal Recruitment Consultant - Clinical Development. This is a hybrid on-site role in Boston, Massachusetts. Candidates must be local to the Boston area.
Base pay range
$200.00 / hr - $280.00 / hr
Job title
Senior Principal Recruitment Consultant - Clinical Development
Responsibilities
- Provide clinical expertise in ALL (adult and pediatric) to support completion of ongoing studies (e.g., CSR)
- Provide strategic and clinical insights for data generation and potential new study designs
- Collaborate in cross-functional working groups to deliver a strategic plan for internal governance decision making prior to year end
- Support regulatory interaction preparations for new sponsored studies
- Clinical Development Strategy and Execution : provide medical and strategic leadership for all clinical initiatives including supporting regulatory interactions with regulatory affairs and cross-functional representatives
- Develop and lead presentations for internal governance meetings to support timely and efficient decision making
- Coordinate with DMPK teams to understand PK modelling applications for dosing / schedule recommendations
- Perform literature searches and support data generation and key publications
- Support Business Development evaluations of promising late-stage assets under consideration for in-licensing or acquisitions
- Medical Monitor : lead design and execution of clinical trials, ensuring alignment with regulatory requirements and company objectives
- Provide medical monitoring oversight for clinical studies in accordance with GCP
- Review data for critical clinical and / or safety endpoints and consult on medical literature for evidence-based decision-making
- Team collaboration : work with asset teams, clinical sub-teams, regulatory affairs, medical affairs, and commercial teams to ensure alignment and successful product development
- KOL engagement, investigational led studies, and publication support
- Support interactions with KOLs and development of advisory board content
- Other duties as required or directed by the Manager or Functional Management
Qualifications
M.D. required with a strong preference for specialty training and board certification in Medical Hematology / OncologyExperience with Acute Lymphoblastic Leukemia is required3+ years in industry with strong preference for regulatory interactions experienceDemonstrated ability to lead clinical development efforts across phases of development within the Hematology / Oncology spaceExcellent public speaking, writing, and communication skills required. Ability to teach and mentor is also critical and work in a cross-functional collaborative way.Problem solving mindset with the ability to be creative and to execute a vision that seeks to drive innovationAbility to organise and prioritise workstreams and guide teams through challengesExcellent operational execution and ability to meet critical timelinesTeam player with strong matrix working capabilityProven track record practicing sound medical judgment as it relates to clinical acumen and risk assessment including leading cohort safety evaluation meetings in early phase studies, co-authoring investigator brochures, and providing clinical expertise on PV-related documentsCore competencies : Leadership, Execution, Strategy, CollaborationSeniority level
Mid-Senior levelEmployment type
ContractJob function
Health Care ProviderIndustries
Pharmaceutical Manufacturing#J-18808-Ljbffr