Project Manager - HEOR - SLR

10 Hours ago • 4-8 Years

Job Summary

Job Description

This Project Manager role requires a dynamic professional with experience in evidence generation and synthesis within the pharmaceutical industry or a related consulting/vendor environment. The role involves offering advanced business solutions in Health Economics and Outcomes Research. Responsibilities include planning, executing, and managing research activities such as literature reviews and assessments of HTA submissions. Additional duties involve data analysis, report writing, and project management. The ideal candidate will be proficient in project management, medical writing and should possess strong communication skills and the ability to work in a global team environment.

Must have:

Experience in evidence generation/synthesis.
Ability to offer advanced business solutions.
Plan, execute and manage research activities.
Expertise in designing and managing systematic review studies.
Proficiency in data collection, processing, and analysis.
Experience with PUBMED, Cochrane, and Embase.
Knowledge of Endnote and RefMan.
Project management skills.
Excellent communication skills.

Good to have:

Authored manuscripts/poster presentations.
Expertise in medical writing.
Experience with the OViD platform.
Expertise in varied therapeutic areas.

4 skills required

4 skills required for this role

Add these skills to join the top 1% applicants for this job

communication

presentation-skills

ms-office

team-management

Job Details

A dynamic and proactive professional with experience in evidence generation/synthesis (literature review), either in a pharmaceuticals company or in a consulting/vendor organization. Should have demonstrated the ability to offer advanced business solutions in the Health Economics and Outcomes Research domain. Strong business & client orientation.

Educational Qualification- Bachelor’s/Master’s degree (with/without PhD) in pharmaceutical science or any relevant life sciences field

Typical Experience ~

4-8 years of experience with proven ability to plan, execute and manage day-to-day research activities involved in evidence-generation studies such as targeted/systematic literature review, assessments of HTA submissions, and other life-sciences research projects

Desirable: Authored a few manuscripts/poster presentations on SLR

The ability to provide integrated value driven insights, solutions and strategic guidance

Expertise in designing, planning, executing and managing systematic review studies in healthcare domain.
Identifying, collecting, processing, analyzing and cataloguing data according to established protocol, procedures & standards, as appropriate to specific objectives of the research study.
Experience on PUBMED, Cochrane, Embase; experience on OViD platform will be a plus
Qualitative and quantitative synthesis of the collated data, along with report writing.
Quality assessments of the identified studies.
Comprehensive knowledge of Endnote, RefMan
Expertise in medical writing would be an additional advantage.

Project management skills
Develop proposals and study protocols
Excellent, communication skills-both written and verbal to engage in discussions with clients, both prior to receiving and during execution of a project
Ability to multi-task, work in a demanding global team environment, work under tight deadlines
Expertise in varied therapeutic areas

Skilled in MS Office including comprehensive knowledge of PowerPoint and having excellent presentation skills.

Soft Competencies

Maturity
A strong outcomes and solution orientation
Comfortable with handling multiple clients/multiple projects
Good business sense: Understand the client’s business imperatives
Team Management

Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.