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 LLCBoston, MA, 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 • Boston, MA, United States

    Related jobs
    • Promoted
    Associate Director / Director, Regulatory CMC

    Associate Director / Director, Regulatory CMC

    Scorpion TherapeuticsBoston, MA, United States
    Full-time
    This position is a key leadership role for the development of the In Vivo franchise at CRISPR.Reporting to the Head of Regulatory Affairs CMC, you will work closely with cross-functional teams and ...Show moreLast updated: 23 hours ago
    • Promoted
    Associate Director, Global Regulatory Affairs CMC Devices and Combination Products

    Associate Director, Global Regulatory Affairs CMC Devices and Combination Products

    AstraZeneca GmbHBoston, MA, United States
    Full-time
    The Associate Director of Global Regulatory Affairs Chemistry, Manufacturing, and Controls (GRA‑CMC) Devices and Combination Products plays a pivotal role in implementation of global CMC regulatory...Show moreLast updated: 25 days ago
    Associate Director, Regulatory Affairs

    Associate Director, Regulatory Affairs

    Rhythm PharmaceuticalsBoston, MA, US
    Full-time
    Quick Apply
    Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases.We develo...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Global Regulatory Affairs, Advertising and Promotion

    Associate Director, Global Regulatory Affairs, Advertising and Promotion

    Takeda PharmaceuticalCambridge, MA, US
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Tak...Show moreLast updated: 5 days ago
    • Promoted
    Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead

    Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead

    TakedaBoston, MA, United States
    Full-time
    Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead.Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead. At Takeda, we are a forward‑l...Show moreLast updated: 23 days ago
    • Promoted
    Associate Director, Global Regulatory Lead, Oncology

    Associate Director, Global Regulatory Lead, Oncology

    Takeda PharmaceuticalBoston, MA, US
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Tak...Show moreLast updated: 5 days ago
    • Promoted
    Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead

    Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead

    Takeda PharmaceuticalBoston, MA, US
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Tak...Show moreLast updated: 5 days ago
    • Promoted
    Associate Director, Regulatory Affairs – Contract

    Associate Director, Regulatory Affairs – Contract

    Nuvation Bio, Inc.Boston, MA, United States
    Full-time
    Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change...Show moreLast updated: 19 days ago
    • Promoted
    Director, Regulatory Affairs - Strategy

    Director, Regulatory Affairs - Strategy

    Lantheus BrandBedford, MA, US
    Full-time
    Director, Regulatory Affairs - Strategy.Lantheus (NASDAQ : LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow d...Show moreLast updated: 30+ days ago
    • Promoted
    • New!
    Global RA Leader - Rare Disease Regulatory Strategy

    Global RA Leader - Rare Disease Regulatory Strategy

    Zevra Therapeutics, Inc.Boston, MA, US
    Full-time
    A rare disease therapeutics company is seeking a VP, Head of Regulatory Affairs to oversee global regulatory strategy and execution. The candidate will lead major submissions and foster team growth ...Show moreLast updated: 16 hours ago
    • Promoted
    Director, Global Regulatory Lead - Oncology

    Director, Global Regulatory Lead - Oncology

    TakedaBoston, MA, United States
    Full-time
    At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and oth...Show moreLast updated: 22 days ago
    • Promoted
    • New!
    Associate Director, Contract Manufacturing

    Associate Director, Contract Manufacturing

    Massachusetts StaffingBoston, MA, US
    Full-time
    Associate Director, Commercial Drug Product Manufacturing And Packaging.Japan with operations in the U.With several marketed products and a diverse pipeline of early- to late-stage investigational ...Show moreLast updated: 7 hours ago
    • Promoted
    Associate Director Regulatory Strategy

    Associate Director Regulatory Strategy

    EPM ScientificBoston, MA, United States
    Full-time
    Associate Director of Regulatory Strategy.A rapidly growing pharmaceutical company is expanding its regulatory leadership team and seeking a strategic, execution-oriented.Associate Director of Regu...Show moreLast updated: 6 days ago
    • Promoted
    Associate Director / Director, Regulatory CMC

    Associate Director / Director, Regulatory CMC

    CRISPR TherapeuticsBoston, MA, United States
    Full-time
    This position is a key leadership role for the development of the In Vivo franchise at CRISPR.Reporting to the Head of Regulatory Affairs CMC, you will work closely with cross-functional teams and ...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Global Regulatory Lead, Oncology

    Associate Director, Global Regulatory Lead, Oncology

    TakedaBoston, MA, United States
    Full-time
    By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Tak...Show moreLast updated: 4 days ago
    • Promoted
    Associate Director, SAP Applications

    Associate Director, SAP Applications

    LantheusBedford, MA, United States
    Full-time
    Lantheus (NASDAQ : LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcome...Show moreLast updated: 11 days ago
    • Promoted
    • New!
    Associate Director, Regulatory Affairs

    Associate Director, Regulatory Affairs

    Massachusetts StaffingBoston, MA, US
    Full-time
    Associate Director Regulatory Affairs.Japan with operations in the U.With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate disco...Show moreLast updated: 8 hours ago
    • Promoted
    Global Regulatory Affairs Device Lead (Associate Director)

    Global Regulatory Affairs Device Lead (Associate Director)

    Sanofi, MA, United States
    Full-time
    Job title • • : Global Regulatory Affairs Device Lead (Associate Director) • Serve as GRA Device Lead on assigned project teams (early phase, late stage and marketed products) • Provide regulatory guida...Show moreLast updated: 24 days ago