The Director/Senior Director Clinical Development at Roivant Sciences will provide clinical scientific leadership for programs, including direct responsibility for clinical development strategy and execution of clinical trials, with a focus in immunology, rare diseases, and oncology. This role involves hands-on design and execution of clinical trials, developing and implementing clinical strategies, and working closely with cross-functional teams and external experts. The position is instrumental in supporting the growth of Roivant’s portfolio and the generation of new portfolio companies.

DIRECTOR/SENIOR DIRECTOR CLINICAL DEVELOPMENT (REMOTE)

Director/Senior Director Clinical Development

Westat is seeking a highly motivated and experienced Associate Vice President with strong business development, client management, project leadership, and clinical research experience to join the leadership team in the Clinical Research Practice. This role involves spearheading business development in clinical research, managing large-scale projects, and securing contracts with federal agencies, specifically targeting the Department of Health and Human Services. The position is remote and focuses on growing the company's clinical research services within HHS agencies.

ASSOCIATE VICE PRESIDENT, CLINICAL RESEARCH (CLINICAL TRIALS) REMOTE

Associate Vice President, Clinical Research

The Medical Director Clinical Programs at Elevancehealth is a remote, individual contributor role responsible for designing and implementing clinical programs with specific medical condition focus for all lines of business enterprise wide. This role involves analyzing data, partnering with leaders to ensure alignment with health priorities, and collaborating on clinical programs that support providers in value-based payment arrangements. The position is 50% UM support and 50% focused on West Region Star related work.

MEDICAL DIRECTOR CLINICAL PROGRAMS (US)

Medical Director Clinical Programs

HealthCare Support is seeking a Director, Clinical Analytics to oversee complex clinical analytics projects, inform business decisions, and manage, develop, and train staff members. This role involves monthly reporting and auditing, testing and implementing for value-based payment models, and managing a team of 16-19 staff members remotely.

DIRECTOR, CLINICAL ANALYTICS

Director, Clinical Analytics

Jazz Pharmaceuticals' Information Services (IS) department is seeking an Associate Director, R&D IS Business Partner within the R&D IS function. This role serves as a strategic partner and trusted advisor to assigned Research & Non-Clinical Development (RNCD) functions, focusing on creating and maintaining the IS strategy and roadmap aligned to business goals. The position involves leading the delivery of the roadmap, ensuring effective adoption of new solutions, managing operational support activities for IS systems, and promoting operational efficiencies and best customer experiences.

ASSOCIATE DIRECTOR, IT BUSINESS PARTNER, DRUG DEVELOPMENT - REMOTE

Associate Director, IS Business Partner Research and Non-Clinical Development

Greenbrook Medical is seeking a Senior Director of Clinical Operations to lead and expand their successful clinical model across Tampa Bay and beyond. This role involves designing, refining, and optimizing clinical workflows, working closely with the Chief Medical Officer, and leveraging a partnership with Tampa General Hospital to scale high-quality care. The ideal candidate will have a strong leadership background, a track record of clinical team development, and the ability to manage key performance indicators to drive excellence in clinical services.

Head of Operations

Senior Director of Clinical Operations

The Associate Director, Clinical Safety MD at Planet Pharma is responsible for supporting safety monitoring and risk management activities for products in development. This role involves working closely with a senior physician and other CSPV staff, as well as cross-functional Safety Management Team (SMT) members. The position is remote and requires candidates to be based in the EST/CST time zone.

ASSOCIATE DIRECTOR, CLINICAL SAFETY MD

Associate Director, Clinical Safety MD

The Clinical Research Associate at Ascendion is responsible for managing clinical activities at study sites, fostering strong relationships within the organization, and overseeing the performance of appointed study sites. This role involves conducting site visits, monitoring, communication, and delivering on assigned study sites, serving as a liaison between Clinical Operations and study site personnel.

Clinical Research Associate

The Director of Lab Services Development at Jones Lang LaSalle will play a crucial role in the growth and development of the company's life sciences business. This strategic position involves liaising with managing directors and account leaders to ensure successful, accelerated growth, focusing on the development of business aligned to organic growth through the management of product delivery and renewal activity. The role also includes tactical responsibilities such as building strong relationships with the Client Growth Sales team and the WD Products and Solutions Development organizations to ensure appropriate and robust products and technologies are proposed.

DIRECTOR OF LAB SERVICES DEVELOPMENT

Director of Lab Services Development

I am excited to partner with a top client on their search for a Vice President, Scientific Director to join their growing team. This role involves leading and overseeing designated accounts, providing scientific and communication support in commercial and scientific affairs, and acting as the leading scientific input for clients. The position is part of a global Medical Communications network, offering a full-service agency capability with an unparalleled, boutique agency service. This role is ideal for someone looking to advance their career in a dynamic work environment.

VP, SCIENTIFIC SERVICES - MEDICAL COMMUNICATIONS - EAST COAST, REMOTE

Vice President, Scientific Director

The Associate Director, Clinical Monitoring Oversight at True North Consulting is responsible for overseeing and implementing a global sponsor oversight monitoring program within the clinical operations department. This role involves leading internal process improvements related to monitoring quality and data integrity, ensuring compliance with regulatory requirements and GCP, and managing a global sponsor oversight monitoring team. The position is remote with possible quarterly meetings in Waltham, MA.

ASSOCIATE DIRECTOR, CLINICAL MONITORING OVERSIGHT

Associate Director, Clinical Monitoring Oversight

The Associate Director, Seramount Research Insights at EAB will play a crucial role in developing research agendas, designing research projects, and producing syndicated research and high-value services for senior executives. This position involves leading strategic research projects from conception to completion, conducting in-depth interviews, performing data and root-cause analyses, and presenting findings to executive-level clients. The role is open to remote employment within the continental U.S. and includes 10% expected travel.

Associate Director, Seramount Research Insights

As an Associate Director of Study Feasibility at AbbVie, you will be part of the Clinical Development Operations team, focusing on clinical trial operations globally. This role involves partnering with study teams to advise on design feasibility, including country and site selection, protocol review, and patient burden assessment. It requires expert facilitation, influence without authority, and strong experience in clinical study design, operations, and management.

Associate Director, Study Feasibility

The Associate Director, Global Pharmacovigilance Quality Management at Sarepta Therapeutics will lead assigned Pharmacovigilance (PV) quality management activities globally for all investigational and marketed Sarepta products. This role requires a collaborative leader with strong systems-thinking and quality management skills. The incumbent will facilitate strategic PV quality planning, lead the implementation and maintenance of a comprehensive PV training program, manage projects using industry-standard project management methods, and oversee PV CAPA and deviation processes, among other responsibilities.

ASSOCIATE DIRECTOR, GLOBAL PHARMACOVIGILANCE QUALITY MANAGEMENT

Associate Director, Global Pharmacovigilance Quality Management

The company is seeking a dedicated MD or DO to join their team as a Principal Investigator for clinical trials in women's health. This role is ideal for a full-time physician looking to diversify their income and provide additional support to their patients through clinical research. The position offers a flexible time commitment, competitive compensation, and the opportunity to enhance patient care through participation in cutting-edge clinical research.

Principal Investigator (MD/DO) for Clinical Trials

Principal Investigator for Clinical Trials

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