Clinical Trial Patient Engagement Associate

Medasource; Indianapolis (IN); On-site; USD 60,000 - 75,000; Full time

Job summary

Medasource in the United States seeks a Clinical Trial Patient Engagement Associate to support design strategy for patient recruitment and retention within our PEER team. The Associate will help translate patient and researcher voices into actionable strategies across clinical programs.

You will collaborate with PEER and CDDA colleagues to deliver strategic direction, and help create deliverables such as patient-facing content and novel recruitment approaches while maintaining key platforms and

Qualifications

• Bachelor's degree in scientific or health related field required.
• Minimum 1 year experience in pharmaceutical industry or equivalent.
• Understanding of the drug/device development process.
• Proven ability to deliver to timelines.
• Excellent communication skills (written and verbal).
• Demonstrated organizational and critical thinking skills.
• Ability to lead and influence toward a common goal.

Responsibilities

• Support the design strategy for clinical programs where the voice of the patient and researchers are represented.
• Support the creation of the design strategy for patient recruitment and retention with the assigned area(s) of focus.
• Partner with PEER team colleagues and CDDA functions to deliver strategic direction for each clinical program.
• Support the creation of deliverables (novel recruitment, patient facing content) in partnership with PEER team colleagues and owners/vendors.
• Understand capabilities and access points to maintain key platforms and systems for the PEER team.
• Contribute to a culture of partnership and shared learning across the PEER team and CDDA to identify best practices.
• Work with PEER team members to evolve internal standards, processes, tools, and best practices.
• Continuously assess evolving partner needs that could be addressed by process improvements or automation.
• Provide strategic and technical support to ensure processes are integrated within CDDA functions.
• Support the delivery of right-sized design strategies for clinical programs.

Skills

Excellent written and verbal comms

Proven ability to deliver to timelines

Organizational and critical thinking

Ability to lead and influence

Education

Bachelor's degree in scientific or health related field

Job description

The Clinical Trial Patient Engagement Associate is responsible for supporting the design strategy for for patient recruitment & retention within our clinical programs. The Associate will have assigned area(s) of focus (e.g., novel recruitment, patient facing content) within the Patient Engagement, Enrollment, and Retention (PEER) team. This role is responsible for supporting different design strategies in alignment with clinical and functional counterparts to gain efficiencies and speed.

Responsibilities:

Support the design strategy for clinical programs where the voice of the patient and researchers are represented

• Support the creation of the design strategy for patient recruitment and retention with the assigned area(s) of focus (e.g., novel recruitment, patient facing content).
• Partner with PEER team colleagues and appropriate Clinical Design Delivery & Analytics (CDDA) functions to deliver the best strategic direction for each clinical program.
• Support the creation of the appropriate deliverables (e.g., novel recruitment, patient facing content) in partnership with PEER team colleagues as well as the functional owners and/or vendors.
• Understand specific capabilities and access points to maintain key platforms and systems in support of the PEER team based upon the assigned area(s) of focus

Ensure continuous improvement by understanding the external needs and challenges of patients and researchers in addition to the internal needs and challenges of our clinical programs

• Contribute to a culture of partnership and shared learning across the PEER team and broader CDDA to identify best practices and standardized approaches to processes.
• Work closely with PEER team members to continue to evolve internal standards, processes, tools, and best practices.
• Continuously assess and evaluate evolving business partner needs that could be addressed by process improvements, standardization, or automation.

Contribute to a team culture that is valued for strategic and technical leadership

• Provide strategic and technical support to ensure that processes for the assigned area(s) of focus are well integrated within the appropriate CDDA functions.
• Support the delivery of right-sized design strategies that can be successfully implemented in our clinical programs.

Qualifications:

• Bachelors Degree in scientific or health related field or equivalent
• Minimum of 1 year experience in pharmaceutical industry or equivalent
• Understanding of the pharmaceutical drug/device development process
• Proven ability to deliver to timelines
• Excellent communication (written and verbal) skills
• Demonstrated organizational and critical thinking skills
• Ability to lead and influence toward a common goal