SSU & REGULATORY SPECIALIST WITH EXPERIENCE IN CLINICAL TRIALS-CLIENT BASED MEXICO-CDMX

Description SSU & Regulatory Specialist with experience in clinical trials-Client Based Mexico-CDMX  Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
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 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.
Job responsibilities  JOB SUMMARY Performs assigned activities within the country that lead to start-up of investigative sites in all phases of  clinical trials.
Responsible for the delivery, with oversight from the SSU Country Manager in one or more  of the following functional areas.
investigator site contracts, ethics and regulatory submissions, and of  essential documents required for site initiation.
Ensures local activities are undertaken in accordance  with agreed timelines, allocated budgets, and required quality standards.
Ensures an efficient start-up  process on assigned studies.
May act as main contact with Regulatory Authorities (RA) and  Central/Regional Ethics Committees (ECs).
nder the supervision of the Project Lead (PL) or Site Start-up  Lead (SSUL) as appropriate, may directly interact with Customers regarding requirements from RA or other local regulatory party.
Accountable to the PL/SSUL at the project level and line manager for  deliverables.
JOB RESPONSIBILITIES  General – Responsible for providing quality on deliverables at the country level and follows  project requirements and applicable country rules, with oversight from the SSU Country Manager.
 Works within the forecasted submission/approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted  timelines are not reached provides clear rationale for delays, assists with contingency plan to  mitigate impact, and escalates the issue as soon as identified.
 Monitors basic financial aspects of the project and the number of hours/tasks available per  contract; escalates discrepancies in a timely fashion.
 Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WIs)  in a timely manner, keeps training records updated accordingly and ensures timesheet  compliance.
 Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company  SOP/Sponsor requirements.
Responsible for one or more of the following functions at the country level.
 Local Submissions Specialist - Follows the project direction provided by the designated country  start-up advisor (CSA) and SSUL.
May serve as a point of contact for the SSUL/PM (or  designee) during start-up on allocated projects.
Compiles and/or reviews essential document  packages for site activation and may also be involved in essential document collection from site.
 Prepares and submits Central EC Applications, Local EC Applications, RA Applications, and  other local regulatory authorities or hospital approval submissions as required and under  supervision.
Prepares ongoing submissions, amendments, and periodic notifications required by  central and local EC and RA, and other local regulatory authorities as needed within the country;  includes safety notifications as required by local rules, with overight from the SSU Country  Manager.
 Local Site ID and Feasibility Support – Provides support with site selection lead and PM/SSUL to  ensure that the appropriate sites are selected for individual studies based on the requirements of  the clinical trial.
 Local Investigator Contract and Budget Negotiator – Supports the SSUL to agree on country  template contract and budget.
Assists in producing site-specific contracts from country template.
Under supervision assist in negotiations of budget and contract with site and via Site Contracts  Service Centre and SSUL lead with Sponsor until resolution of issues and contract execution.
Assists with quality control and arranges execution of CTAs as well as archival of documents into  repositories and capture of metadata Qualifications What we’re looking for Get to know Syneos Health 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 Sites and + 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.
QUALIFICATION & REQUIREMENTS (please indicate if ‘preferred’)  Associate’s Degree or equivalent combination of education and training.
 Good understanding of clinical trial process across Phases II-IV and ICH GCP, Ability to interact  effectively and appropriately with investigative site personnel.
 Good organizational skills and good attention to detail, with proven ability to handle multiple tasks  effectively.
 Ability to take direction from multiple individuals and set priorities accordingly.
 Ability to effectively communicate across multiple function groups (clinical team, PM, Director).
 Demonstrated ability to work independently, as well as part of a team.
Utilize problem-solving  techniques effectively.
 Quality-driven in all managed activities.
 Flexibility and willingness to adapt to rapidly changing environment and learn/perform new  functions.
 Strong computer skills, including Word, Excel, PowerPoint, Publisher #LI-RR1