Job Overview:
Are you a postdoctoral fellow who is passionate about providing culturally-sensitive and strength-based mental health services to diverse young adults? Do you want to build your own practice while completing your licensure requirements? If so, you might be the ideal candidate for our team at Deeply Rooted Psychological Services LLC!
About Us:
Deeply Rooted Psychology is an innovative therapy practice that provides compassionate and culturally-sensitive mental health services to diverse populations in Wilmington, Delaware. We specialize in supporting young adults and those in life transitions with anxiety, depression, trauma, and other common struggles. We are looking for a therapist who can join our team of professionals and contribute to the growth of our company. We are looking for a postdoctoral fellow who can join our team and grow with our innovative company.
Responsibilities:
- Authors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports and documents to support meetings with regulatory agencies) in partnership with key stakeholders
- Serves as the lead Medical Writing for complex or pivotal clinical studies for multiple programs or therapeutic areas
- Provides expert review of study-level and program-level documents
- Participates in developing key messages for complex clinical regulatory documents
- Provides leadership on teams responsible for defining the direction and regulatory strategy for a clinical development program
- Provides strategic and scientific contributions to regulatory documentation in support of the clinical development pipeline
- Contributes to content and strategy of presentations for regulatory agency advisory committee meetings; may prepare advisory committee briefing documents
- Ensures document preparation is compliant with company and industry standards
- Strong contributor on cross-functional teams working on standard operating procedures, process improvements, and integration of new tools and technologies
Knowledge and Skills:
- Outstanding written and oral communication skills
- Extensive experience writing and editing clinical regulatory documents
- Ability to analyze, interpret, and summarize highly complex data
- Advanced understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminology
- Ability to mediate conflicts by negotiating, compromising, persuading, and facilitating the open exchange of ideas and opinions
- Highly developed project management and organizational skills
- Ability to manage challenging, high-value projects
- Initiative and creativity in solving complex problems; ability to have a substantial role in developing and implementing improvements in cross-functional processes
- Serves as the lead Medical Writing for complex or pivotal clinical studies for multiple programs or therapeutic areas
- Provides expert review of study-level and program-level documents
- Participates in developing key messages for complex clinical regulatory documents
- Provides leadership on teams responsible for defining the direction and regulatory strategy for a clinical development program
- Provides strategic and scientific contributions to regulatory documentation in support of the clinical development pipeline
- Contributes to content and strategy of presentations for regulatory agency advisory committee meetings; may prepare advisory committee briefing documents
- Ensures document preparation is compliant with company and industry standards
- Strong contributor on cross-functional teams working on standard operating procedures, process improvements, and integration of new tools and technologies
Qualifications:
- Master’'s degree is required.
- Minimum of 2+ years related experience is preferred.
- 3+ years in a Medical Education role is favorable.
- Proficient with Microsoft Office, including Outlook, Word, Excel and PowerPoint.
- Excellent verbal and written communication skills, with a demonstrated ability to communicate clearly and professionally.
- Provides expert review of study-level and program-level documents
- Participates in developing key messages for complex clinical regulatory documents
- Provides leadership on teams responsible for defining the direction and regulatory strategy for a clinical development program
- Provides strategic and scientific contributions to regulatory documentation in support of the clinical development pipeline
- Contributes to content and strategy of presentations for regulatory agency advisory committee meetings; may prepare advisory committee briefing documents
- Ensures document preparation is compliant with company and industry standards
- Strong contributor on cross-functional teams working on standard operating procedures, process improvements, and integration of new tools and technologies
Benefits:
- Competitive pay and bonuses. Will receive regular clinical supervision.
- Flexible schedule, with weekday, evening, and weekend hours available.
- Ideal for early career psychologists seeking support and guidance in a private practice setting.
- Training in how to be a supervisor (if interested).
This is a full-time position, requiring a commitment of 40 hours per week. The term of the contract is 1 year. The job location is remote, with headquarters in Wilmington Delaware.
We look forward to hearing from you and considering you for this exciting opportunity to make a positive difference in the lives of young adults! Please submit your CV and cover letter.
Job Type: Full-time
Benefits:
- Professional development assistance
Experience level:
Schedule:
Application Question(s):
- Do you have a Doctoral Degree in Psychology from an accredited doctoral program in the US? or Did you complete an APA-accredited Pre-doctoral internship?
- Do you have experience providing culturally-sensitive clinical services and strength-based therapeutic services?
Education:
Ability to Relocate:
- Wilmington, DE 19803: Relocate before starting work (Required)
Work Location: Hybrid remote in Wilmington, DE 19803