As a member of ONO Group
Associate Director, Clinical Science
Location
Massachusetts
Posted
4 days ago
Salary
$171K - $236K / year
Seniority
Senior
Job Description
Associate Director, Clinical Science
Deciphera Pharmaceuticals
• The Associate Director Clinical Scientist contributes to the execution of the clinical development plan for candidate drug products in collaboration with Project Leaders and Medical Directors. • The clinical scientist will be involved in operationalizing studies, monitoring data in real time to ensure the integrity of the study and proactively identifying issues in the conduct of trials. • Responsible for medical review and data analysis for the purposes of both data cleaning and interpretation for regulatory documents and publications. • Monitoring of clinical data: Perform high level clinical data review for quality and patient safety on an ongoing basis and escalate issues to the medical director as appropriate. • Work collaboratively with data management, clinical operations, and medical monitors to ensure clinical data review is performed efficiently and in alignment with the needs of the trial. • Generate and review clinical documents including concept sheets/decks, clinical study protocols, investigator brochures, and regulatory documents. • Organize and present data, study designs, and other information to advisory boards, investigator meetings, site interactions, study committees, and other internal and external settings.
Job Requirements
- PhD or equivalent plus 5+ years of experience or bachelor/master’s degree plus 10+ years of experience postgraduation that includes pharmaceutical industry experience in clinical drug/biologics development and the associated regulatory processes.
- Strong organizational skills to ensure that necessary data collection and documentation are accomplished for the required analysis and interpretation of clinical trial results.
- Ability to interact with internal team members and external partners effectively.
- Experience with clinical data analysis.
- Ability to influence decision-making within a multidisciplinary team in areas of expertise.
- Excellent communication and presentation skills.
- Business Travel: up to 20% business travel may be required.
- Experience across Phase I-III drug development trials is preferred, with a focus on product development in Hematology-Oncology and/or rare disease.
Benefits
- Competitive salary and annual bonus.
- Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
- Generous parental leave and family planning benefits.
- Outstanding culture and opportunities for personal and professional growth.
Related Guides
Related Categories
Related Job Pages
More Medical Director Jobs
Endoluminal Program Director – Endoluminal Clinical Sales Director
IntuitiveA global technology leader in minimally invasive care and the pioneer of robotic-assisted surgery.
• Recruit, develop, and lead a high-performing Endoluminal Clinical Sales team across the Europe Direct Region. • Drive execution of the Ion commercial strategy to achieve and exceed procedural growth, revenue, and organizational goals. • Coach and support Endoluminal Program Managers (EPMs) in performance management of QBR/ETA teams. • Foster a culture of accountability, collaboration, innovation, and continuous improvement aligned with Intuitive's mission and values. • Drive strong cross-functional collaboration and alignment across teams. • Maintain team focus and commitment to the defined Ion commercial strategy. • Partner closely with Endoluminal Sales Directors (ESDs) and Endoluminal Sales Managers (ESMs) to deliver best-in-class customer experience and maximize customer success. • Develop and maintain strategic relationships with physician leaders, executive stakeholders, and key opinion leaders to accelerate market adoption and advocacy. • Identify, scale, and implement best practices, programs, and processes that support accelerated growth of the Ion procedure business. • Effectively allocate and leverage organizational resources to achieve commercial objectives while maintaining budget discipline. • Drive a solution-focused culture in a dynamic and challenging environment.
Senior Director, Vaccines Retail Channel Medical Lead
PfizerPfizer is a leading biopharmaceutical company headquartered in New York, New York. Over the years, Pfizer has received numerous awards and accolades for its bus
• The Senior Director, Vaccines Retail Channel Medical Lead is a senior, field‑based medical leader within the Vaccines Field Medical organization, responsible for enterprise‑level medical engagement across the U.S. retail pharmacy and retail healthcare channel. • Support the development and delivery of objective, scientifically sound medical information tailored to national retail partners, addressing Pfizer’s vaccines and the diseases they prevent. • Collaborating closely with cross-function medical partners to identify vaccine specific medical education and project needs. • Compliantly execute mutually beneficial, retail stakeholder‑specific medical projects, collaborations, strategic medical partnerships, and non‑interventional studies that align with vaccine‑specific business and public health needs. • Build and sustain strategic, longitudinal medical partnerships with national and regional retail pharmacy chains and retail healthcare organizations that influence vaccination delivery models, access strategies, and population‑level immunization outcomes.
Executive Director, Clinical Platforms, Product Development
FortreaFortrea is a contract research organization (CRO) that provides advanced laboratory-focused services that help change lives. On a mission to deliver “life-cha
• Define and execute the clinical platforms product strategy and roadmap, aligned to Fortrea’s enterprise and clinical delivery objectives. • Lead end-to-end product development lifecycle, including ideation, engineering, validation, deployment, and lifecycle management of applications. • Drive adoption of a product-centric operating model (agile, DevOps, customer-first delivery). • Ensure solutions are scalable, secure, and compliant with regulatory requirements within clinical research. • Evaluate and integrate digital health, AI/ML, and emerging technologies to enhance clinical trial and delivery and patient experience. • Continuously evaluate market trends, competitive landscape, and technology trends to ensure Fortrea maintains competitive position in the marker. • Lead the day-to-day operating model for Clinical Platforms, ensuring delivery predictability, quality, and efficiency. • Own PMO governance, portfolio prioritization, and execution discipline across platform initiatives. • Establish consistent delivery standards, reporting cadence, and performance metrics. • Proactively identify and mitigate risks, dependencies, and resource constraints. • Ensure alignment between product roadmaps and delivery capacity. • Drive continuous improvement in delivery speed, cost efficiency, and quality outcomes. • Ensure platforms support the end-to-end clinical trial lifecycle, including study startup, site management, data capture, monitoring, safety, and regulatory submission. • Translate clinical and operational needs into technology-enabled solutions that improve efficiency, compliance, and data integrity. • Act as the primary integrator across Clinical Operations, Commercial, Quality, Regulatory, Security, and Data Privacy. • Partner with business leaders to ensure clear accountability, governance, and decision-making across complex initiatives. • Own development of executive-level communications, presentations, and external-facing materials. • Build and maintain a standardized library of platform assets (decks, demos, one-pagers).
Medical Science Liaison
Revolution MedicinesRevolution Medicines (RevMed) is committed to revolutionizing treatment for patients with RAS-addicted cancers, specializing in oncology drug discovery and development. With the mi
Role Description We are seeking a highly motivated field medical professional to join our team as Medical Science Liaison, Oncology, UK. This role will execute approved field medical plans within an assigned UK territory, engage in peer-to-peer scientific exchange with healthcare professionals, gather and communicate medical insights, support clinical study site and investigator engagement, and contribute to medical education, advisory boards, and congress activities under the direction of the Medical Director, UK. Medical Science Liaisons (MSLs) are an essential member of the Medical Affairs team who will work as an extension of the Medical Affairs organization. The MSL team will serve as a key liaison between Revolution Medicines and healthcare professionals. Within an assigned geographic territory, the MSL will be responsible for: - Cultivating and strengthening professional relationships with key opinion leaders (KOLs), healthcare providers, and academic centers of excellence involved in various phases of product development. - Collaborating with stakeholders within medical affairs and across the organization, including but not limited to Clinical Development, Commercial, Program Management, Clinical Operations, and Compliance teams. The ideal candidate is an effective communicator, driven, detail-oriented, proactive, and a skilled collaborator. The role is an individual contributor position with no direct line-management accountability. The MSL contributes field insights and scientific expertise to support the Swiss medical plan but does not own country medical strategy, governance, budget, or team leadership. Qualifications - Advanced life science degree (PhD, MPharm, MD, or MSc). - 8+ years of relevant experience in Medical Affairs, Field Medical, Clinical Development, or a similar role within the pharmaceutical or biotech industry; prior MSL experience in Switzerland strongly preferred. - Proven experience as an MSL or similar medical affairs role, ideally within oncology. - Strong understanding of clinical research methodologies and drug development processes. - Knowledge and experience within the oncology therapeutic area, preferred experience in lung and gastrointestinal cancers. - Excellent verbal and written communication skills. - Proven ability to analyse and synthesize scientific information effectively. - Excellent presentation skills, with the ability to effectively communicate complex scientific data to diverse audiences. - Strong networking skills with proven ability to successfully build and maintain relationships with KOLs and healthcare professionals. - Self-directed and able to thrive in a fast-paced and dynamic environment. - Willingness to travel up to 60% of time. Requirements - Develop and maintain strong relationships with KOLs, healthcare professionals, and academic institutions to advance scientific and medical knowledge. - Communicate clinical and scientific data to KOLs and healthcare professionals through presentations, educational programs, and scientific discussions. - Collect, document, synthesise, and communicate field medical insights from KOLs and HCPs to the Medical Director and relevant internal teams. - Provide scientific support for medical congresses, advisory boards, and other relevant scientific engagements to enhance the visibility of Revolution Medicines within the scientific and medical communities. - Establish credibility as a scientific expert and resource for internal stakeholders, providing medical and scientific support for assigned products and therapeutic areas and territory. - Collaborate cross-functionally with Medical Affairs, Clinical Development, Commercial, Clinical Operations, and Compliance to support execution of approved medical strategies and tactics. - Stay current with scientific literature, emerging research, and competitive landscape. - Adhere to Revolution Medicines Core Values and policies. - Understand the regulatory requirements for customer engagement by field-based employees. - Develop and execute the field medical engagement plan for assigned accounts and stakeholders. - Maintain high-quality documentation of scientific interactions and insights in accordance with company systems and compliance requirements. - Support onboarding and informal coaching of new field medical colleagues, where appropriate. - Provide territory-level input to medical planning, launch readiness, and external engagement priorities. Benefits - Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. - We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy.



