Junior Clinical Investigator

SGS

• $80K — $95K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD, M.D., D.O., or similar post-graduate degree in Science, Medicine, or Engineering required
  • 7-10 years of experience in a related field
  • Dermatology background, especially in sunscreen and cosmetic testing, is advantageous
  • Proven ability to manage multiple projects effectively
  • Strong coordination skills in a fast-paced environment.

Responsibilities

  • Oversee clinical research of consumer products involving healthy paid volunteers
  • Write protocols and analyze study data to prepare reports
  • Develop and maintain Standard Operating Procedures (SOPs)
  • Supervise studies to ensure compliance with protocols and SOPs
  • Protect the rights and welfare of research subjects
  • Interface with sponsors, IRBs, and various stakeholders for documentation
  • Manage study team and training of personnel

Benefits

  • Medical, dental, and vision insurance; life insurance; employee assistance programs
  • 401(k) with company match and immediate vesting
  • Access to online training courses and classroom development experiences
  • Tuition reimbursement program
  • Paid time off and family leave to promote work-life balance
Full Job Description
Job Description

The Jr. Clinical Investigator, CRS oversees the clinical research of consumer products involving healthy paid volunteers. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures, good clinical practice and FDA regulations.
  • Oversees the clinical research of consumer products involving healthy paid volunteers.
  • Writes protocols, collects and reviews data, prepares progress reports, analyzes results, writes summaries and conclusions and issues reports.
  • Develops, maintains and reviews Standard Operating Procedures (SOPs). Ensures that study personnel have access to SOPs and that SOPs are followed.
  • Conducts and / or supervises studies in accordance with the protocol and SOP's.
  • Protects the rights, safety and welfare of subjects.
  • Interfaces with the Sponsor, staff, contractors, professional societies, Institutional / Investigational Review Board (IRB), subjects, government agents / agencies and other business units. Obtains appropriate information, documentation and signatures.
  • Notifies the Sponsor and / or IRB of any changes to or deviations from the protocol and document changes and deviations.
  • Delegates duties, as appropriate. Ensures that all individuals working on the study have necessary credentials, are adequately trained, understand their obligations and are properly supervised.
  • Provides a sufficient number of trained staff members to be assigned to each study. Maintains training records of staff members.
  • Ensures that the Informed Consent (IC) is clear and accurate so that subjects can understand the IC. Provides the opportunity for subjects to ask questions about the IC. Ensures that subjects have signed the IC.


Qualifications
  • Must possess a PhD, M.D., D.O., or similar post-graduate degree in Science, Medicine, or Engineering
  • 7+ years of experience in a related field
  • Dermatology background, sunscreen and cosmetic testing experience a plus
  • 10+ years of experience in a related field
  • Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.


Additional Information

Our Benefits

We care about your total well-being and will support you with the following, subject to your location and role.
  • Health: Medical, dental and vision insurance, life insurance, employee assistance programs.
  • Wealth: In addition to base pay, we offer 401(k) with company match (immediate vesting upon enrollment).
  • Happiness:
    • Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement program
    • Work-Life Balance: Paid-time off and family leave

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