Manager - Clinical Trials

SDG MGMT Company • Hackensack, NJ

1d • Onsite

About The Position

Full-Time Clinical Research Coordinator in our Englewood Cliffs Office. The Clinical Trials Manager oversees the planning, execution, and monitoring of clinical research studies to ensure compliance, quality, and adherence to protocols within healthcare settings.

Requirements

• Skill in exercising initiative, fair judgment, problem solving, and decision-making.
• High level of critical thinking and “outside of box” solutions.
• High level of patience and great interpersonal skills to have high level of effectiveness with employees and provider.
• Understanding of cosmetic and dermatologic practices from conception to completion including protocol design, informed consent design, clinical trial design, study advertising, IRB communication, and randomize patient participation.
• Understanding of drug development process.
• Knowledge of concepts of clinical research and drug development.
• Ability to understand scientific and medical information.
• Quick learner and detail oriented with interest in learning new concepts/skills.
• Experience working with IRBs and handling investigational product.
• Adaptable for various work conditions, and functions well under tight or limited deadlines.
• Capable of taking basic vitals (i.e blood pressure, temperature, respiration rate, pulse, etc.).
• Competencies in and essential skills in the following: cross functional relationships, communication, decision making, execution/results/process improvement, interpersonal skills and training skills.
• Demonstrated strengths in the following areas: Planning, organizational, project management and analytical skills.
• Oral and written communication.
• Time management.
• Negotiation.
• Conflict management and resolution.
• Problem solving.
• Attention to detail.
• Interpersonal and networking skills.
• Relationship building.
• Motivational Skills
• Cross-cultural sensitivity
• Customer Service Orientation
• Advanced computer skills (word processing, spreadsheets, graphics, presentation slides, electronic data capture)

Responsibilities

• Attend investigator meetings as required. Some travel necessary/required.
• Assure patients are scheduled and seen according to protocol requirements.
• Monitor patient visits and progress throughout the study and routinely inform the principle investigator(s) of patient study status and new updates.
• Document date drug/devices and supplies received: Store drug in locked drug room Label drug storage area (shelf) with correct number Order additional drug/supplies as needed.
• Prepare subject files CRF Consent Lab/Test requests Source documents and clinic binder/chart/other.
• Work with the chosen IRB
• Complete necessary subject data according to the submitted protocol by pharmaceutical company.
• Train and supervise coordinators
• Multitask between multiple projects and offices and follow through with all ongoing tasks and/or office needs.
• Recruitment of patients for randomization into studies.
• Assist in any special projects Operations Team needs assistance with.
• Contributes to team effort by accomplishing related results as needed.
• Maintain a high level of clinical care at SDG and assure that best clinical practices are communicated.

Benefits

• Medical ( Virtual Care included)
• HSA/FSA
• Dental
• Vision
• 401K
• Company Sponsored Short Term Disability ( Only applicable for non-California employee )
• Pre-tax savings available for public transit commuters
• Your birthday is an additional personal holiday
• Employee discounts on Schweiger skin care products & cosmetic services

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: No Education Listed