Associate Director - Clinical Scientist
Associate Director Clinical Scientist
Salary: $185,000 - $205,000
New York City or Jersey City (Hybrid)
Job Description
Founded by a team of noble prize winning scientists, EPM is partnered with one of the most exciting and cutting edge biotech companies in the industry. They have raised over $1 billion dollars of funding to advance their pipeline of 7 programs and are gearing up for their first Phase 3. Focusing in oncology, they are using a first of it's kind drug discovery platform that has allowed them to create the most innovative drugs ever seen.
Responsibilities
* Serve as the lead clinical scientist on the trial team, overseeing specific aspects of clinical and scientific execution for clinical protocols
* Guide the medical monitoring team in evaluating and interpreting clinical data and protocol deviations, collaborating with Clinical Research and Pharmacovigilance
* Partner with various departments to develop protocols and related study materials (e.g., informed consent forms, amendments), and coordinate with Clinical Operations on study deliverables
* Ensure case report forms (CRFs) are designed to align with protocol requirements, working closely with Clinical Data Management and Programming
* Collaborate across functions to monitor clinical data, ensuring the quality, completeness, and integrity of trial conduct
* Mentor other clinical scientists on tactical and scientific matters
* Assist in the creation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (authoring documents and preparing slides as needed)
* Apply analytical skills to understand program objectives and design impacts on data analysis; identify risks and develop mitigation strategies
* Promote consistent medical and clinical data review techniques across studies and programs'
Qualifications
* 10+ years of experience with a Bachelor's degree, or 8+ years with a postgraduate degree
* Experience in clinical drug development, or a PhD, Pharm D, or RN degree is preferred
* Strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
* Ability to manage multiple priorities with effective planning, time management, and prioritization skills
* Strong analytical skills to interpret clinical trial data and draw conclusions
* Scientific expertise to propose, design, and execute clinical research and development studies, and author documents related to clinical trials (e.g., medical monitoring plans, statistical analysis plans, informed consent forms, clinical study reports)
* Ability to interact with key stakeholders across Clinical Development functional areas
* Proactive approach, strategic thinking, and leadership in driving clinical study goals
* Ability to influence opinions and decisions of internal and external stakeholders across functional areas
* Problem-solving, prioritization, conflict resolution, and critical thinking skills
* Strong communication, technical writing, and presentation skills
* Experience in oncology is preferred
Benefits
* Medical
* Dental
FAQs
Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.
Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.
We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business.Â
That's why we recommend registering your resume so you can be considered for roles that have yet to be created.Â
Yes, we help with CV and interview preparation. From customized support on how to optimize your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.