Study Manager

Study Manager

August 10, 2022 By

Introduction:

Welcome to dicentra!

We are a diverse team from a wide range of industries and backgrounds all united by one common passion: to improve the health and wellness of people around the world. Whether we are developing and executing a break-through clinical trial, issuing the required certifications to sell a product in a new country or jurisdiction, or guiding a client to help them successfully navigate through regulatory hurdles, we do it with confidence, knowing that our team is backed by incredible and wide-ranging experience and one of the highest success rates in the business. If you share our passion for improving health and wellness and want to find purpose in your work, apply now and join one of North America’s most respected brands in both the Health Sciences and Food industries.

Let’s build a better world, together!

Why join us

Best Workplace 
We nourish an environment devoted to honesty and fairness, trust and respect. We care deeply for our team members and take work-life balance seriously, allowing our people to decide on a schedule that best fits their life and working preferences.

Best People 
We unite cross-industry professionals with a shared passion for improving people’s health and wellness. Our inspiring leaders are accessible and work eagerly side-by-side with individual employees to help them understand and achieve their objectives.

Best Opportunities 
We encourage our team members to continuously develop and enhance their skills and expertise. We recognize and reward courageous choices and innovative ideas that result in the growth of our people and company, and the success of our clients.

Become a part of a purpose-driven and future-oriented business that impacts and improves millions of lives worldwide!

Responsibilities:

  • Monitor and report on the progress of delegated clinical trials.

  • Prepare, oversee, and review documents that are related to the assigned clinical study.

  • Ensure the availability of necessary resources for the execution of clinical projects by working with the Project Managers.

  • Review invoices being presented by study vendors and external consultants with CT Supervisor.

  • Assess the requirements, supplies and other pre-requisites for conducting the clinical trial.

  • Help in the training and development of clinical staff as per the protocol.

  • Oversee the pattern and manner in which a clinical research study is being conducted.

  • Resolve concerns/queries identified by the study monitor and liaise with PI to ensure clinical trials are conducted efficiently.

  • Work hand-in-hand with appropriate clinical trial team members to manage study IPs/IDs, documents, templates, logs, etc. that are related to the clinical study.

  • Perform other clinic duties as assigned.

  • Will be the primary contact between the study monitor and the clinic team.

Qualifications 

  • Bachelor’s degree in Sciences, Health Sciences or Nursing.

  • Minimum of 2 years of related work experience.

  • Preference will be given to candidates with industry experience in a clinical research environment.

  • Exceptional interpersonal communication skills, professionalism and work ethic.

  • Ability to work individually and as part of a team in a dynamic, including the ability to motivate and organize a diverse team.

  • Accountable and accurate, with a strong sense of attention to detail.

  • Comfortable handling important and private information while multi-tasking and working in a fast-paced environment.

  • Must be able to work with little to no supervision, within strict deadlines, as well as balance multiple projects simultaneously.

In addition to the skills and qualifications above, we value the following qualities in all of our team members:

  • Personality is characterized by high-quality standards, responsibility and engagement.

  • Ability to interact with a range of personalities and many levels of the organization.

  • Demonstrated self-motivation and the ability to take initiative.

  • Project management and strong prioritization skills.

  • Attention to and ability to execute details.

  • Adaptable to changing environment, client and project needs.

Job Type: Full-time.  

Location: Toronto, ON office.

Applying:

To be considered for future opportunities, please email your cover letter, resume/CV, and any related supporting documentation to hr@dicentra.com with “Study Manager” in the subject line.

As part of the hiring process, in addition to interviewing, successful candidates may be required to complete a skills assessment and a reference/background check. If you are sent a skills assessment, please complete it for consideration for the advertised position.

We thank all applicants for their interest, however, only those selected for an interview will be contacted.