Sago

Market Research

ProjectManager

Managua, Managua, Nicaragua FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Project Manager at Sago. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement, market research, clinical research. managing all aspects of Clinical market research projects accurately with internal/external clients. determine business/project problems”

What You'll Achieve.

establish project objectives; maintain quota; impact on study objective

Industry & Context.

Market Research
Problems you'll solve

determine business/project problems

Eligibility Requirements

Travel to assigned destinations to execute clinical research study, meet with clients, or provide trainings.

What They're Looking For.

Must Have

Minimum of 4+ years in a market research or clinical environment, knowledge of clinical practices, Bachelor’s degree required, Excellent oral and written communication skills, interpersonal abilities, Maintain the highest level of professionalism at all times, Ability to effectively engage respondents and secure their cooperation, client service orientation, In-depth knowledge of clinical research practices, advanced industry knowledge in clinical research and data collection, Deep understanding of departmental roles, processes, and functions, ability to apply this knowledge to benefit clients and staff, Adaptable, ability to work both independently and collaboratively within a team, Proven ability to multitask, thrive in a fast-paced environment, Proficiency in Microsoft Office, Proficiency in Excel

Nice to Have

Master’s preferred

What You'll Do.

managing all aspects of Clinical market research projects accurately with internal/external clients

determine business/project problems

establish project objectives

analyze and oversee data collection for clinical surveys

close contact with the client

making sure the client is fully aware of project status

addressing any changes in a timely and satisfactory manner

Completes all required trainings as well as any required certifications GCP (Good Clinical Practice)

CITI (Constructive Industry Training Institute) etc.

implement and ensure project execution according to study protocol and Sago’s Quality Management System Standards

specifically applicable core or support procedures as identified in training.

Manage quality of work for projects to include but not limited to: development and review of study materials and project attend project update lead study work with Call Center on recruitment of maintain quota and validate work according to guidelines.

Maintain positive subject/respondent relationships to support ongoing participation in research project.

Complete any required reporting as specified daily/weekly

keeping the Clinical team (Sales/ VP – Lead) informed of any project issues that have impact on study objective

including but not limited to: subjects/respondent participation

or financial results.

Responsible for subject/respondent management in accordance of project specifications.

Execute trainings as identified in the protocol.

Utilize Sago’s Clinical data management and reporting systems.

Execute Participant Interviews via phone or in person.

Travel to assigned destinations to execute clinical research study

or provide trainings.

Assist in writing Protocols

working with the sponsor

and submitting documents to the IRB (Institutional Review Board).

Perform site certifications and perform site audits.

Responsible to deliver client ready deliverables such as cross tabs

How You'll Work.

Team & Collaboration

cross-functional coordination; work both independently and collaboratively within a team; keeping the Clinical team (Sales/ VP – Lead) informed of any project issues

Communication Scope

Excellent oral and written communication skills; interpersonal abilities; client service orientation; client communication

Process & Methodology

process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement, project objectives, project status, project execution, project issues, project specifications

Full Job Description

The Project Manager is responsible for managing all aspects of Clinical market research projects accurately with internal/external clients. The manager will determine business/project problems and establish project objectives. The Project Manager will analyze and oversee data collection for clinical surveys. This position demands close contact with the client, making sure the client is fully aware of project status, and that any changes are addressed in a timely and satisfactory manner. * Completes all required trainings as well as any required certifications ie; GCP (Good Clinical Practice), CITI (Constructive Industry Training Institute) etc. * Understand, implement and ensure project execution according to study protocol and Sago’s Quality Management System Standards, specifically applicable core or support procedures as identified in training. * Manage quality of work for projects to include but not limited to: development and review of study materials and project schedule; attend project update meetings; lead study briefings; work with Call Center on recruitment of participants; maintain quota control; and validate work according to guidelines. Maintain positive subject/respondent relationships to support ongoing participation in research project. * Complete any required reporting as specified daily/weekly, keeping the Clinical team (Sales/ VP – Lead) informed of any project issues that have impact on study objective, including but not limited to: subjects/respondent participation, timelines, quality, or financial results. * Responsible for subject/respondent management in accordance of project specifications. * Execute trainings as identified in the protocol. * Utilize Sago’s Clinical data management and reporting systems. * Execute Participant Interviews via phone or in person. * Travel to assigned destinations to execute clinical research study, meet with clients, or provide trainings. * Assist in writing Protocols, working with the sponsor, and submitting d

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