Senior Research Associate - Strategic %26 Scientific Affairs

SENIOR RESEARCH ASSOCIATE – STRATEGIC & SCIENTIFIC AFFAIRS
*We are looking to fill this role in North America.

The Real-World Evidence team supports biopharmaceutical companies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients in the pharmaceutical/ biotechnology/ medical device industries build economic and epidemiological evidence to demonstrate and support the value of their products. Through analysis of large health administrative databases (e.g., medical claims, electronic health records, registries, etc.), we may provide key information such as:

Treatment patterns and drug utilization
Resource utilization
The incidence and prevalence of diseases and co-morbidities
The incidence of adverse events
The impact of various risk factors
Cost-effectiveness
Burden of disease
Comparative effectiveness data

Position Overview:
The Senior Research Associate drafts project deliverables, interacts with clients, and contributes to strategic thinking under the direction of senior staff. Supports scientific coordination and project management, including scoping, tracking progress, and coordinating team tasks for multiple projects.

Essential Duties and Responsibilities (other duties may be assigned):
The Senior Research Associate in Data Collection will bear scientific responsibility for the design and implementation of de novo data collection studies (retrospective, prospective, and/or cross-sectional) under oversight of more senior staff.

In particular, the Senior Research Associate will:

• Provide scientific guidance/consultation on scientific methodological and operational considerations of study design and conduct
• Lead on or oversee the development of draft scientific project deliverables (e.g., protocols, analysis plans, case report forms (electronic or paper), survey questions, reports) for senior review.
• Interact directly with study sponsors, physician experts, and clinical sites
• Assist the responsible scientist with monitoring project budget spend and managing timelines for scientific tasks/deliverables.
• In some client engagements, serve as Principal Investigator, with final responsibilities for project budget, deliverables and timelines
• Draft project deliverables (e.g., protocols, analysis plans, reports,) for senior review, and draft abstracts and manuscripts as lead or co-author
• Contribute to the growth of Evidera through business development activities, including support of proposal development, participation in the sales cycle, conference attendance, and presentations
• Support other organizational activities as needed (e.g. supervise and/or mentor junior staff; closely collaborate with other project stakeholders such as clinical operations, data management, biostatistics, and data analysts; contribute to development of training materials and process improvements)
• Travel (national and international travel) is expected

Consulting Expectations:

• Participates in client calls and is expected to be able to address questions posed directly to him/her about his/her work
• Contributes to strategic thinking under the direction of senior staff.

Managerial Duties: May possibly mentor or manage more junior staff or practice area interns

Education, Professional Skills & Experience:

• PhD (epidemiology or closely related field) or MSc with relevant experience
• Experience with de novo data collection (field) studies (non-interventional designs in particular)
• Good understanding of epidemiologic methodology
• Previous experience in consultancy and/or CRO environment highly desirable
• Working knowledge of MS Office software; working knowledge of data analysis software (e.g., SAS, Stata, R) a plus
• Experience with design of peri- or post-approval late phase interventional studies is not required but would be considered a plus

Personal Skills & Competencies:

• Demonstrated ability to communicate and document information effectively in written English, including the ability to produce scientific reports, presentations, emails and other written deliverables that are well-organized, free from errors, and are appropriately adjusted to the characteristics and needs of the audience.
• Strong organizational, time-management, prioritization and decision-making skills necessary to evaluate, plan and accomplish multiple work goals in a timely fashion.
• Able to quickly learn and apply new information, skills and procedures.
• Proactive and positive approach to tasks and projects, as well as resilience when encountering process, project, budget or client changes that are inherent in the consulting environment.
• Strong communication and interpersonal skills including the ability to quickly develop and sustain positive rapport with internal and external contacts in person, over the phone and by email.
• Experience presenting ideas to individuals and groups in a formal presentation setting
• Delivers a positive internal/external client experience; listens and understand the client's needs, and recommends solutions
• Demonstrates sound professional judgment in analyzing, responding to, and resolving enquiries, issues and escalations.

Who we are?
Evidera is a business within in Pharmaceutical Product Development, LLC (PPD) a leading global contract research organization (CRO), and a is a preeminent provider of evidence-based solutions. We provide integrated scientific expertise and global operational capabilities to help clients generate the evidence needed to optimize the market access and commercial potential of products.

Working Environment:
PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
Able to communicate, receive and understand information & ideas with diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary for typical working hours.
Ability to use and learn standard office equipment and technology with proficiency.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
May require travel.

What we offer?
We know that if you are provided with the right support and resources needed you will thrive! Therefore, Evidera offers a great mix of compensation and benefits options to show you how valuable you are to the organization.

Some of our perks include:

• Highly competitive salary and bonus structure
• Generous benefits package, including healthcare, dental, vision and paid time off to spent with your friends and family
• Flexible working environment by offering fully remote work for most of our positions, to support work-life balance
• Clear opportunities for growth and career progression. We offer multiple Learning & Development programs, coaching and mentoring trainings, career planning and discussions to help you grow as a professional.
• Access to Employee Well-being programs and services. We value your emotional health and offer a variety of programs to support your mental healthcare.
• Collaborative working environment with focus on Diversity and Inclusion. At Evidera, we respect one another and recognize that our diversity makes our business stronger. We strive to be an inclusive organization where colleagues can be their authentic selves and grow their careers.
• Global exposure: Opportunity to work on multiple projects with some of the industry’s leading researchers around the globe.
• Smooth onboarding process with your own dedicated onboarding specialist and a working buddy to help you navigate through your first few weeks thus ensuring great start to your new role.

Our 4i Values:
Our 4i Values are critical components in accomplishing our mission. These values guide us and, ultimately, define us.

Integrity – Innovation – Intensity – Involvement

If you resonate with them and wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!*

• only shortlisted candidates will be contacted

#LI-REMOTE