Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical Trial & Pharmacovigilance Manager

VENESCO LLC

Job Description

Job Description

Description:

  Clinical Trial & Pharmacovigilance Manager

Venesco LLC is seeking a Clinical Trial & Pharmacovigilance Manager to lead clinical operations and drug safety surveillance activities across multiple FDA-regulated clinical development programs. This individual will provide strategic oversight for clinical trial execution, adverse event management, safety surveillance, and regulatory compliance while leading multidisciplinary teams.

Requirements:

 

Duties and Responsibilities  

  • Direct Phase I and Phase II clinical trial operations. 
  • Lead pharmacovigilance and safety surveillance activities. 
  • Develop and maintain product safety profiles. 
  • Oversee adverse event collection, coding, review, and reporting. 
  • Manage DSMB activities and implementation of recommendations. 
  • Ensure compliance with FDA, ICH, and sponsor requirements. 
  • Coordinate safety reviews, risk assessments, and signal detection activities. 
  • Lead development of safety management plans and surveillance plans. 
  • Manage cross-functional teams including monitors, safety personnel, and clinical operations staff. 
  • Support INDs, Investigator Brochures, DSURs, annual reports, and safety submissions. 
  • Develop SOPs and improve operational processes. 

Minimum Qualifications  

  • Advanced degree in Clinical Research, Nursing, Pharmacy, Public Health, or Life Sciences. 
  • Minimum 10 years of clinical research experience. 
  • Demonstrated leadership of Phase I and Phase II clinical studies. 
  • Strong expertise in ICH-GCP and FDA clinical research requirements. 
  • Experience managing clinical operations and pharmacovigilance programs. 
  • Proven ability to lead multidisciplinary teams. 

Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit

Vacancy posted 9 days ago
Similar jobs that could be interesting for youBased on the Clinical Trial & Pharmacovigilance Manager in Frederick, MD vacancy
  •  ...Job Description Job Description Description: Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance with approved... 
    Suggested

    VENESCO LLC

    Frederick, MD
    9 days ago
  • A leading biotechnology company in Frederick, Maryland, is looking for a Delivery Lead to oversee testing and quality control processes. The ideal candidate has 2+ years in biotechnology or Quality Control, with strong knowledge of GMP and SOPs. This contract position involves...
    Suggested
    Contract work

    Integrated Resources, Inc ( IRI )

    Frederick, MD
    1 day ago
  • $69.55k - $125.73k

     ...communication skills. Strong scientific writing skills. Exceptional attention to detail. Excellent organizational and time management skills. Proficiency with Microsoft Word, Excel, and PowerPoint. Experience using IT data management systems. If you're... 
    Suggested
    Contract work
    Work at office
    Local area
    Remote work
    Flexible hours
    3 days per week

    Leidos

    Frederick, MD
    7 days ago
  • Leidos is seeking a Biomedical Life Scientist in Frederick, MD to provide scientific and meeting support for the CDMRP. This hybrid role requires in-person work at the Frederick office at least three days per week with some local travel in the DC/Baltimore area. Responsibilities...
    Suggested
    Work at office
    Local area
    3 days per week

    Leidos

    Frederick, MD
    1 day ago
  • Leidos seeks a Biomedical Life Scientist in Frederick, MD to support CDMRP in a hybrid role requiring 3 days in the office with some local travel. The role involves planning and documenting scientific meetings, recruiting scientists, drafting meeting materials, and analyzing...
    Suggested
    Work at office
    Local area

    Leidos LLC

    Frederick, MD
    14 hours ago
  • Leidos Health & Services Division in Frederick, MD, is seeking a Biomedical Life Scientist for hybrid work with in-person presence at the Frederick office at least three days per week. The role supports CDMRP meetings and related programs, requiring strong scientific writing...
    Work at office
    3 days per week

    Via Logic LLC

    Frederick, MD
    2 days ago
  • Leidos Inc. in Frederick, Maryland seeks a Biomedical Life Scientist to support CDMRP by planning and executing scientific meetings, recruiting experts, and drafting meeting materials. This hybrid role requires a minimum of 3 days/week in the Frederick, MD office and some...
    Work at office
    Local area
    3 days per week

    Leidos Inc

    Frederick, MD
    1 day ago
  • $227.6k - $341.4k

     ...Affairs to maintain audit readiness Program & Product Lifecycle Management Lead CDx programs from concept through development,...  ...Proven experience developing and validating assays to support clinical studies Experience participating in regulatory audits and agency... 
    Work at office

    Precisionmedicinegroup

    Frederick, MD
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical Trial & Pharmacovigilance Manager. Be the first to apply!