Screening Supervisor

Altasciences

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profile Job Location:

Quebec - Canada

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

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 youre a recent college graduate or seeking your next career opportunity its time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About The Role

The Supervisor Screening Department will organize clinical trial screening activities and is responsible for the supervision and coordination of the screening team ensuring screening activities are conducted within trial timelines. The Supervisor Screening Department will ensure tasks performed and screening activities are executed in compliance with study protocol Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

What Youll Do Here

  • Management of the screening team including but not limited to PTO management timesheet approval on-going and yearly performance reviews employee hiring training and training records disciplinary actions and termination.

  • Provides comments on protocol during internal review and participates in protocol meetings

  • Ensure the creation and review of study specific documents training or other materials as needed for study specific procedures.

  • Conduct protocol training and/or coordinate any required training(s) on study specific procedures.

  • Hold meetings with Screening Team members to communicate clinical trial needs and/or departmental objectives.

  • Attend sponsor initiation meetings and audits.

  • Ensure the confidentiality of clinical trial participants and sponsors is respected.

  • Manage staff scheduling and ensure staffing needs are met.

  • Oversee and/or track the completion of regulatory documentation (i.e. DOA protocol training) to ensure staff are trained prior to performing clinical trial-related screening activities.

  • Maintain and advocate a high level of customer service and quality within the department.

  • Work with management to track trend and/or report KPIs as a measure of success.

  • Assist with or coordinate and communicate with Marketing teams as required.

  • Perform technical screening activities including but not limited to screening data collection safety measurements (ECG vital signs etc.) sample handling processing and in-house testing.

  • Handle communications with vendors and resolve any related issues.

  • Ensure the resolution of data queries in a timely manner.

  • Reviews and reports protocol/SOP deviations expediently.

  • Participate in SOP revisions.

  • Obtain track and/or treat volunteer complaints.

  • Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.

  • Other tasks as assigned by management.

What Youll Need to Succeed

  • High School diploma required and related job experience; college degree preferred.

  • Minimum of 5 years of related experience in the healthcare field.

  • Minimum of 3 years of supervisory or team leader experience.

  • Cardiopulmonary resuscitation (CPR) certification.

  • Expertise with Microsoft Office strong computer literacy.

  • Excellent written and verbal communication in French and English.

  • Leadership interpersonal and organizational skills.

  • Well developed interpersonal skills are required.

  • Personal/professional integrity and proven discretion in handling confidential information.

  • Capable of managing multiple conflicting priorities and working in a fast-paced environment.

  • Must be self-directed motivated and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.

  • Leadership interpersonal and organizational skills.

  • Candidates must be available between 9am and 7pm.

  • Flexibility to work overtime when necessary.

  • Usually one Saturday out of two (sometimes on Sundays).

Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Supervisor Screening Department including but not limited to for the following reasons:

  • The requirement to have study protocols designs and clinical research documents written and documented in English as required by industry regulatory agencies.

  • The employee communicates frequently with Altasciences employees across Canada and the United States. As such English is the main language used to correspond between offices.

  • The employee frequently communicates with English-only customers outside the province of Quebec.

What We Offer

  • Full time position (375 hours/week).

  • On site position at our Montreal office (1100 Beaumont); accessible by public transportation (Metro LAcadie) and free parking lot for employees.

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

  • 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 Reviews

#LI-JG1

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!


Required Experience:

Manager

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-b...
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Contract research organization specialized in seamless, end-to-end, early phase drug development, we act to get your most promising compounds into and through early phase clinical trials.

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