Associate Director Clinical Research Jobs in New York

At least two years of experience as a clinical research associate

Excellent writing, editing, and communication skills

Strong Administrative and Organizational skills to support several team members

A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences

Familiarity with various computer document formats, styles, and standards

· Collecting, analyzing, and recording data

People Management Skills: Experience managing direct reports.

Project Management Skills: Experience managing multiple projects or tasks under deadlines.

Data Skills: Ability to manage, analyze, and draw interpretations from large datasets in Microsoft Excel.

Partnership Skills: Experience working across departments, preferably within the context of empowering non-data people to embrace research and evaluation.

Knowledge of the Field of Education: Understanding of the education landscape, including early education, higher education, and workforce development

Knowledge of the Field of Education:

Leads and develops contracts, Invoices, and Finances related to procedures and protocols for Global team for 7-10 projects.

Monitors and oversees study requirements are conducted, including ensuring the study inclusion/exclusion factors, products, time points, and panelists are included.

Advanced Clinical/Science degree or professional credentials required (BS, MS, PhD, PharmD, and/or scientific background/experience)

Rele ant transferable experience (clinical practice, clinical or scientific training, academic research, and regulatory/scientific).

Experience in Medical/Cosmetic Dermatology, Plastic Surgery, Cellular Biology, and/or Facial Aesthetic disciplines strongly desired.

Strong analytical skills and presentation skills

Previous experience of sharing knowledge, key learnings and best practice from experiences on the projects that they have been responsible for

Previous experience moderating a range of face-to-face and online sessions, and facilitating both client and consumer workshops

Previous experience of managing and leading end-to-end qualitative projects

Leads and takes responsibility for the successful on-time and on-budget delivery of projects that generate top quality results.

Prepares creative and innovative proposals

• Responsible for study-related contracting, budgets, and vendor/partner management

- 3-5 years HEOR modeling experience

• The incumbent may supervise external vendors or partners to execute these activities

• Maintain awareness of new scientific and methodological developments within therapeutic area

• Present outcomes research data at national and international congresses and publish articles in scientific journals.

Experience moderating qual research methodologies, interviews, focus groups, facilitation, design thinking, etc.

Experienced working in the CPG or pack design space

Knowledge of design thinking and what makes good design

Ability to project manager and work in a boutique environment

Research Manager / Associate Director of Research

5-8 years working within qual research, insights, and/or brand strategy

Strong organizational and time-management skills.

Collaborate with cross-functional teams to ensure the successful execution of clinical trials, including data management, biostatistics, and medical writing.

Perform site qualification, initiation, and close-out visits, including site selection, site initiation, and site closure.

Identify and escalate study issues to the appropriate stakeholders, including the clinical project manager, medical monitor, and regulatory affairs.

Minimum of 2 years of experience as a CRA in the biotechnology or pharmaceutical industry or academic space

Experience in oncology and solid tumors is required.