Postdoctoral Research Fellow contributing to NIH-funded R01 study on mobile app-based mindfulness intervention for spinal cord injury and chronic pain patients.
Locations (4)
Jacksonville, Florida, United States
Phoenix, Arizona, United States
Scottsdale, Arizona, United States
Rochester, Minnesota, United States
Responsibilities
Contribute to implementation of the research protocol and development of study procedures, training materials, and assessment workflows.
Collaborate with research coordinators to support participant recruitment, engagement, retention, and completion of study assessments.
The Clinical Research Associate II serves as the primary site contact throughout all phases of clinical research studies, ensuring compliance with regulations and contributing to the success of clinical trials.
Responsibilities
Independently manage clinical trial sites from initiation through close-out.
Conduct on-site monitoring visits, including SQV, SIV, Routine Monitoring, and Close-Out Visits.
Ensure compliance with protocols, ICH-GCP, sponsor requirements, and local regulations.
Review source documents and study data to ensure quality and patient safety.
Identify, escalate, and resolve site-related issues and risks.
Requirements
Bachelor's degree
Nice to have: Experience in CROs
Nice to have: Experience in pharmaceutical companies
Nice to have: Experience supporting audits and inspections
Nice to have: Experience across multiple therapeutic areas
Develop and maintain strong relationships with investigational sites throughout all phases of the clinical trial lifecycle.
Perform site management and monitoring activities in accordance with ICH-GCP guidelines, Sponsor SOPs, local laws and regulations, study protocol requirements, and site monitoring plans.
Gain a comprehensive understanding of study protocols and related procedures.
Coordinate and manage site readiness activities in collaboration with cross-functional stakeholders.
Participate in site selection, qualification, and validation activities.
Requirements
Bachelor's Degree or higher in a scientific or healthcare-related discipline
Lead the development and delivery of complex, high-impact scientific publications that communicate clinical and real-world evidence accurately, clearly, and responsibly.
Responsibilities
Lead complex, high-impact publication deliverables and independently manage the end-to-end development, submission, and resubmission of priority manuscripts and congress materials.
Write and critically review manuscripts, abstracts, posters, and presentations covering complex clinical trials, pooled analyses, health economics and outcomes research, and integrated evidence.
Lead disclosures involving integrated datasets, post-hoc analyses, network meta-analyses, conventional meta-analyses, HEOR or epidemiology components.
Partner with biostatistics, clinical, safety, and medical teams to evaluate datasets, clarify analytical methods, and communicate findings appropriately.
Oversee systematic literature searches, evidence synthesis, and gap analyses that support publication planning and future disclosures.
Lead the development and delivery of complex, high-impact scientific publications for AstraZeneca and Alexion.
Responsibilities
Lead complex publication deliverables and manage end-to-end development, submission, and resubmission of priority manuscripts and congress materials
Write and critically review manuscripts, abstracts, posters, and presentations covering complex clinical trials, pooled analyses, health economics and outcomes research, and integrated evidence
Manage publication systems, document versions, comment resolution and integration, dependencies, and collaborator alignment across programmes
Partner with biostatistics, clinical, safety, and medical teams to evaluate datasets and communicate findings
Oversee systematic literature searches, evidence synthesis, and gap analyses
Requirements
Master’s degree in life sciences, pharmacy, biochemistry, biotechnology, pharmacology, public health, or a related discipline
Lead complex publication strategy and writing for AstraZeneca’s high-priority publication programmes, ensuring scientific rigor, ethical compliance, and impactful communication.
Responsibilities
Set publication strategy and guide narratives using multi-study and real-world datasets
Manage customer concerns related to disclosures
Provide end-to-end scientific and delivery leadership for publication programmes
Lead writing and guide review for research papers and symposium content
Set document and evidence strategy for combined data evaluations
Requirements
Master’s degree in life sciences, pharmacy, biochemistry, biotechnology, pharmacology, public health or a related discipline
Nice to have: Advanced degree such as PharmD, PhD, MD or MPH
Nice to have: Experience leading integrated disclosures
Nice to have: Knowledge of therapeutic areas such as Cardiovascular, Renal and Metabolism; Respiratory and Immunology; Vaccines; and Immune Therapies
Conduct protocol-assigned participant interviews and standardized assessments following appropriate training.
Support consistent implementation of study procedures across participating sites, including intervention fidelity and maintenance of study blinding, as applicable.
Evaluate participant engagement with the mobile intervention and help identify barriers to adherence and accessibility.
Requirements
M.D. or Ph.D. (preferably in Psychology or a closely related field)
Nice to have: research experience in clinical, health, or rehabilitation psychology; pain management; or behavioral medicine
Nice to have: experience with randomized controlled trials, digital health interventions, or remotely delivered research
Nice to have: experience interacting with research participants and administering standardized patient-reported assessments
Nice to have: familiarity with REDCap and statistical software such as R, SAS, SPSS, or Stata
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