What are the responsibilities and job description for the Quality Control Tech (Miami, FL - ONSITE) position at Syneos Health?
Description
Quality Control Tech
The quality control technician is responsible for reviewing and verifying the quality and integrity of the generated study data to ensure compliance with the protocol, SOPs, controlled documents, and study related procedures.
Job Responsibilities
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
Position in Canada
This determination ensures the jobholder has sufficient technical ability to perform the role
One to 2 years of relevant work experience would be considered an asset.
Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel and clinical software.
Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
Experience in regulatory context will be considered an asset
Position In Canada
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000 Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health
Quality Control Tech
The quality control technician is responsible for reviewing and verifying the quality and integrity of the generated study data to ensure compliance with the protocol, SOPs, controlled documents, and study related procedures.
Job Responsibilities
- Verify the accuracy of raw data by ensuring the consistency of the sequence of events.
- Communicate information to the responsible person and management in order to ensure the efficiency and the smooth conduct of the project.
- Responsible for documenting queries and ensure the follow-ups for the observations are answered adequately.
- Verify that the SOP and Protocol deviations are accurately documented.
- Ensure the review of required documents for sponsor and/or regulatory agency visits.
- May participate in the training of new employees.
- Act as a resource or employees to ensure that good clinical practice and adequate documentation procedures are adhered to.
- May be assigned other clinical tasks.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Position in Canada
- College degree in Science or other related field
- In lieu of degree, 2 years of experience in related field.
- Associate or bachelor's in science or related field.
- In lieu of degree, 2 years of experience in related field.
This determination ensures the jobholder has sufficient technical ability to perform the role
One to 2 years of relevant work experience would be considered an asset.
Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel and clinical software.
Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
Experience in regulatory context will be considered an asset
Position In Canada
- English level: Required bilingualism includes understanding various messages, exchanging verbally on subjects related to the tasks to be executed, and writing simple messages.
- Spanish level: Required bilingualism includes understanding various messages, exchanging verbally on subjects related to the tasks to be executed, and writing simple messages.
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000 Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health
