Talent.com
No longer accepting applications
Sr Regulatory Associate PM (US or LATAM Based Only)

Sr Regulatory Associate PM (US or LATAM Based Only)

Syneos Health / inVentiv Health Commercial LLCBridgeport, CT, United States
30+ days ago
Job type
  • Full-time
Job description

Sr Regulatory Associate PM (US or LATAM Based Only)

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 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.

Job Responsibilities

  • Fully Remote in US and LATAM Only. Must be eligible to work in US or LATAM without Visa sponsorship in order to be considered.
  • Under limited supervision, performs detailed and confidential project-related duties directly related to regulatory submissions and regulatory compliance.
  • May also perform limited general project administrative
  • duties.

  • Responsibilities typically include creating and editing regulatory reports,
  • summarization of data in the public domain, conduct quality control review of documents, and may also include collection and analysis of data to produce reports to support investigational new drug applications(INDs), new drug applications or new marketing applications (NDAs / MAAs), drug master files (DMFs),

    variations, renewals, marketing authorization transfers (MATs) and other lifecycle maintenance activities.

    JOB RESPONSIBILITIES

    Essential Functions :

    For non-complex submissions, independently fulfill the following responsibilities. For complex submissions, fulfill the following responsibilities under supervision and with guidance from more senior regulatory colleagues :

  • Prepares and submits full application or components of IND, marketing and lifecycle maintenance
  • applications to ensure compliance with government acts and regulations.

  • Undertakes information processing activities with extremely high reliability at high quality and in tight timelines according to standard processes and operating procedures.
  • Undertake project specific activities with minimal supervision from senior colleagues within cost and time estimates / contracts.
  • Preparation of records and / or logs and maintenance or update of regulatory databases as per Syneos Health and / or client requirements.
  • Conducts Quality Control reviews of documents and sends out for review, tracks until final submission or delivery to client.
  • Attends client meetings as needed and builds client relationship in support of projects and deliverables.
  • Systematically reviews Regulatory Associates or other Senior Associate's work, performance, and productivity tracking, coordinating with project manager and director for coordination of the project.
  • Identifies risks to project delivery related to own workload and appropriate escalation. For identified non-complex issues, provide proposals for issue resolution.
  • Assists in training and mentoring of team members depending upon project requirements.
  • Create and Maintain Content Plans within Veeva Vault RIM
  • Translating Smartsheet timelines into Microsoft Project and Veeva Vault RIM
  • Assist with planning, managing, and tracking of regulatory submissions
  • Qualifications - External

    QUALIFICATION REQUIREMENTS :

  • 3-5 years of Regulatory Experience within Industry
  • BS / BA degree or equivalent practical experience.
  • Experience in a work-related area preferred.
  • Excellent interpersonal / communication skills.
  • Advanced skills in Microsoft Office Applications.
  • Strong analytical skills.
  • Ability to work independently and to understand and carry out detailed instructions.
  • Ability to interact with staff from multiple departments.
  • Ability to work concurrently on projects, each with specific instructions that may differ from project to
  • project.

  • Fluent in speaking, writing, and reading English.
  • In-depth understanding of regulatory requirements and guidelines including FDA regulations, EMA guidelines and ICH standards. Keywords : eCTD, NDA, IND, EU CTA, MAA, EU CTR, NDS
  • Additional Information :

    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and / or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills / experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

    At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions / bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. The annual base salary for this position ranges from $47,000-$79,900 USD. The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

    Best,

    At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions / bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

    Salary Range :

    The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

    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 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.

    http : / / www.syneoshealth.com

    Additional Information

    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and / or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills / experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

    Create a job alert for this search

    Associate Regulatory • Bridgeport, CT, United States

    Related jobs
    • Promoted
    • New!
    Associate Scientist

    Associate Scientist

    Planet PharmaNew Haven, CT, US
    Full-time
    Accurately, capture, verify and standardize assay performance data across platforms to support method performance evaluation across global testing network. Interface with laboratory teams, refine da...Show moreLast updated: 21 hours ago
    • Promoted
    OCI AP

    OCI AP

    IBMArmonk, NY, United States
    Full-time
    A career in IBM Consulting is built on trusted relationships and close collaboration with clients across the globe.As an Associate Partner, you will engage with visionary leaders across industries ...Show moreLast updated: 23 hours ago
    • Promoted
    • New!
    Strategic Finance AVP / Associate — FP&A & Analytics

    Strategic Finance AVP / Associate — FP&A & Analytics

    iCapitalGreenwich, CT, United States
    Full-time
    A leading financial services firm is seeking an Associate / Assistant Vice President to join its Corporate Finance team.The role involves strategic finance responsibilities including budgeting, for...Show moreLast updated: 18 hours ago
    Senior Privacy Program Specialist

    Senior Privacy Program Specialist

    Westchester Medical CenterValhalla, New York, United States, 10595
    Full-time
    Senior Privacy Program Specialist.The Senior Privacy Specialist leads advanced efforts to protect patient information and ensure compliance with HIPAA and other privacy regulations across the WMC H...Show moreLast updated: 15 days ago
    • Promoted
    U.S. Banks Conduct Risk Associate

    U.S. Banks Conduct Risk Associate

    Morgan StanleyPurchase, NY, US
    Full-time
    Morgan Stanley Private Bank, National Association ("Bank" or "MSPBNA") provides deposit and lending products and services to serve the needs of Wealth Management clients and seeks a Conduct Risk As...Show moreLast updated: 1 day ago
    • Promoted
    Tax Associate

    Tax Associate

    H&R BlockBridgeport, CT, US
    Full-time
    At H&R Block, we believe in the power of people helping people.Our defining Purpose is to provide help and inspire confidence in our clients, associates, and communities everywhere.We also believe ...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director of the Quinnipiac University Poll

    Associate Director of the Quinnipiac University Poll

    InsideHigherEdHamden, Connecticut, United States
    Full-time
    The Associate Director plays a pivotal role in shaping the strategic direction and execution of the Quinnipiac University Poll. Working closely with the Director, this position ensures the applicati...Show moreLast updated: 30+ days ago
    • Promoted
    Senior Manager, Regulatory Affairs (Biosimilars)

    Senior Manager, Regulatory Affairs (Biosimilars)

    Fresenius Kabi USA, LLCBridgeport, CT, United States
    Full-time
    The Senior Manager, Regulatory Affairs delivers Regulatory Affairs and compliance guidance and strategic input as a subject matter expert in Biosimilar Development and Life Cycle Management to find...Show moreLast updated: 5 days ago
    • Promoted
    • New!
    Tax Senior Associate | Private Equity In-House

    Tax Senior Associate | Private Equity In-House

    CBIZNew Haven, CT, United States
    Full-time
    Tax Senior Associate | Private Equity In-House.Tax Senior Associate | Private Equity In-House.Our growing Alternative Investment Group practice provides tremendous career opportunities in an enviro...Show moreLast updated: 6 hours ago
    • Promoted
    Senior Associate, Corporate Compliance and Transformation Services

    Senior Associate, Corporate Compliance and Transformation Services

    KPMG USStamford, CT, United States
    Full-time
    Senior Associate, Corporate Compliance and Transformation Services.At KPMG, you can become an integral part of a dynamic team at one of the world's top tax firms. Enjoy a collaborative, future-forwa...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director of Transformation (Hybrid)

    Associate Director of Transformation (Hybrid)

    RaytheonUnionville, CT, US
    Full-time
    Associate Director, Strategy & Transformation.The Strategy & Transformation (S&T) team within Enterprise Services (ES) is seeking a highly analytical, business-minded, passionate program leader to ...Show moreLast updated: 2 days ago
    • Promoted
    • New!
    Pharmacy Coordinator - Controlled Substances & Sterile Products

    Pharmacy Coordinator - Controlled Substances & Sterile Products

    White Plains HospitalWhite Plains, NY, United States
    Full-time
    Under the general direction of the Director / Assistant of Pharmacy Services, the Pharmacy coordinator- controlled substance and sterile products provides comprehensive pharmaceutical care and work w...Show moreLast updated: 7 hours ago
    • Promoted
    Senior Associate, Corporate Compliance and Transformation Services

    Senior Associate, Corporate Compliance and Transformation Services

    AECOMStamford, CT, United States
    Full-time
    Business Title : • • Senior Associate, Corporate Compliance and Transformation Services.Requisition Number : • • 119991 - 20. At KPMG, you can become an integral part of a dynamic team at one of the world...Show moreLast updated: 30+ days ago
    • Promoted
    Fund Origination - Associate

    Fund Origination - Associate

    iCapitalGreenwich, CT, United States
    Full-time
    Capital is looking to hire a Fund Origination Associate to support its growing alternative investments direct and registered fund business. This role will report into a Vice President on the Fund Or...Show moreLast updated: 7 days ago
    • Promoted
    Sr Director, Analyst - AI Platforms (Remote : US)

    Sr Director, Analyst - AI Platforms (Remote : US)

    GartnerStamford, CT, United States
    Remote
    Full-time
    Sr Director, Analyst - AI Platforms (Remote : US).Gartner Analysts are industry thought leaders who create must-have research, market predictions, and best practices for a broad range of world‑leadi...Show moreLast updated: 4 days ago
    • Promoted
    Associate Director, Statistical Programming

    Associate Director, Statistical Programming

    InvivydNorth Haven, CT, United States
    Full-time
    Associate Director, Statistical Programming.United States very seriously and we come to work each day on a mission to deliver protection from serious viral infectious diseases, beginning with SARS-...Show moreLast updated: 7 days ago
    Hybrid Senior Associate Level Privacy Law

    Hybrid Senior Associate Level Privacy Law

    Carrie Rikon & Associates, LLC.White Plains, NY, US
    Full-time
    Quick Apply
    Hybrid Law Firm Senior Associate Privacy Salary Range of 150K-210K Plus Yearly Bonus Offered Excellent compensation package plus benefits White Plains, NY A nationally recognized ...Show moreLast updated: 30+ days ago
    • Promoted
    Financial Regulatory Reporting, AVP

    Financial Regulatory Reporting, AVP

    MizuhoGreenwich, CT, United States
    Full-time
    Mizuho Americas Finance - Financial Regulatory Reporting is a team responsible for the preparation of regulatory filings for multiple entities under Mizuho US operations, reporting to Mizuho Americ...Show moreLast updated: 7 days ago