Massachusetts Jobs

Responsibilities in the role

• Ensures proper conduct of clinical trials in accordance with the Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and standards to achieve project goals, timelines and quality

• Accountable for study execution and drives key decisions

• Authors, provides input, and/or oversees program and/or study level

• Provides proper oversight of CROs and other third party vendors to ensure quality of delivery, financial accuracy, and adherence to timelines

• Manages financial aspects of clinical studies

• Assists in development and improvement of Clinical Operations processes and procedures

• Mentors junior staff

• Manages direct reports (if required)

• Involved in interviewing, hiring, and training employees

• Involved in vendor selection including critical review of contracts, and/or work orders and management of ongoing performance.

• Collaborates on SOP development

• Proactively identifies, manages, and escalates issues related to clinical programs

• In collaboration with appropriate study team members, identifies study quality issues and assist with creation and implementation of corrective actions and preventative actions (CAPA) as needed

What your profile could look like:

• Bachelor’s degree Scientific/health care field preferred. Advanced degree preferred.

• Clinical operations experience (8+ years) with evidence of increasing responsibility within a pharmaceutical/biotech company or CRO

• Strong background in project Ability to multi-task and manage workload independently

• Experience leading cross-functional teams

• Ability to work strategically within a business-critical and high-profile development program

• Critical thinking and a good understanding of the scientific and clinical components of studies in therapeutic area.

• Excellent verbal and written communication and presentation skills (English)

• Comfortable in a small company environment that is fast paced, challenging and where all leaders must take on a hands-on approach to get results

• Excited and driven by science and the vision to improve disease management and patient care

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.