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Supervisor, Clinical Operations

AltasciencesAltasciences·Pharmaceuticals / Biotechnology

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Posted

80 days

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About the role

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.  No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About The Role
The Supervisor, Clinical Operations is responsible for the supervision and coordination of Clinical Operations team members and clinical activities during clinical trial execution. The Supervisor, Clinical Operations will ensure clinical activities are completed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.

Schedule:  Monday-Friday 1400-2300 and occasional weekends.


What You’ll Do Here
• Management of the Clinical Operations team, including but not limited to, PTO management, timesheet approval, on-going and yearly performance reviews, employee hiring, disciplinary actions and termination.
• Oversee, manage and/or coordinate the training and training records for the Clinical Operations team.
• Proactively assess learning opportunities for the Clinical Operations team.
• Provide direction to team members during the execution of clinical trial activities.
• Ensure the confidentiality of clinical trial participants and sponsors is respected.
• Maintain and advocate a high level of customer service and quality within the department.
• Perform clinical trial activities, including but not limited to, data collection, safety measurements, sample handling and in-house testing.
• Record adverse events and concomitant medication use and follow-up on on-going adverse events until resolution.
• Provide a continuous line of communication with management teams on the progression of clinical trials.
• May assist in sponsor visits and regulatory audits and ensure the timely resolution to any related findings.
• May assist in the resolution of data queries.
• May participate in SOP and protocol reviews.
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
• Hold meetings with clinical members to communicate clinical trial needs and/or departmental objectives.
 

What You’ll Need to Succeed
• High School diploma or GED and related job experience required; college degree preferred.
• Excellent written and verbal communication (French and English at the Montreal location), leadership, interpersonal and organizational skills.
• Customer service focused, able to work in a fast-paced environment.

What We Offer:

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans

  • 401(k)/RRSP with Employer Match

  • Paid Vacation and Holidays

  • Paid Sick and Bereavement Leave

  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Review 

#LI-TN1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

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Aplyr's read

Altasciences is a dynamic CRO specializing in early-phase clinical trials, attracting professionals committed to advancing pharmaceutical and biotech innovations.

Synthesized from recent postings & public sources

What's promising

  • Altasciences offers comprehensive early-phase clinical development services, providing a crucial role in drug development.
  • The company is expanding, evident from diverse recent hires across scientific, technical, and operational roles.
  • Employees are involved in innovative projects that contribute to significant advancements in pharmaceuticals and biotechnology.

What to watch

  • Working in early-phase trials can involve high pressure due to tight deadlines and regulatory scrutiny.
  • The CRO industry is highly competitive, requiring constant adaptation to new client demands and technologies.
  • Job stability may fluctuate with project-based work typical in contract research organizations.

Why Altasciences

  • Altasciences integrates all early-phase services under one roof, streamlining the drug development process.
  • The company emphasizes a collaborative work environment, fostering cross-departmental learning and innovation.
  • Altasciences' focus on both pharmaceuticals and biotechnology offers diverse career paths within the same organization.

Aplyr’s read is generated by AI from public sources. Was it useful?

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About Altasciences

Altasciences is a full-service contract research organization (CRO) that provides early-phase clinical development services to the pharmaceutical and biotechnology industries.

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