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Manager Ophthalmic Certification Project Management Group

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 
Maryland (USA), United States

Offer summary

Qualifications:

Bachelor's degree or equivalent experience, Minimum 6 years related experience, 3 years in a pharmaceutical/CRO setting, 2 years of supervisory experience, Proficient in MS Office Suite.

Key responsabilities:

  • Oversee training, mentoring and performance management of Project Managers
  • Ensure project deliverables meet budget, schedule and quality standards
  • Coordinate Project Team Meetings and develop agendas
  • Develop client relationships and manage project issues effectively
  • Facilitate the recruitment and retention strategies for the team
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Emmes Research Large https://www.emmes.com/
1001 - 5000 Employees
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Job description

Overview

Job Posting Title

US Remote/Rockville/Frederick

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Manager, Ophthalmic Certification Project Management Group (OCPMG) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical-sponsored clinical trials, as a matrix leader of a vendor project team. The Manager, OCPMG will be client-facing and serve as the internal lead of the project through the life cycle of the study, ensuring effective project delivery in agreement with contracted project timeline and budget. The Manager, OCPMG directs project delivery by driving team and financial efficiency, work product quality, and is responsible for client satisfaction through strong relationship management. The Manager, OCPMG works closely with the Ophthalmic Certification Project Management leadership to ensure compliance with operational tasks, Standard Operating Procedures (SOPs) and overall ophthalmic certification objectives.

Responsibilities

  • Accountable for the training, performance management, and mentoring of assigned Project

Managers.

  • Provides ongoing coaching and feedback to Project Managers, including addressing

performance issues, conducting formal performance appraisals, and creating development

plans. Escalates performance issues to Director, Ophthalmic Project Management.

  • Coordinates Project Team Meetings, including the development of meeting agendas and

minutes.

  • Ensures training occurs and evaluates proficiency or additional training needs of Project

Management (PM) staff.

  • Tracks PM utilization with the goal to ensure at least 90% utilization of all staff.
  • Motivates and develops the team.
  • Develops and oversees recruitment and retention strategies for the Ophthalmic Certification

Project Management Group. 

  • Serves as the primary point of contact for biopharma clients and demonstrates proficiency in

knowledge and understanding of client needs.

  • Ensures that deliverables for the assigned projects are completed according to the contract

budget, schedule, and quality standards. Projects will be effectively managed in all areas of

performance.

  • Develops successful working relationships with clients, executive management, and project

staff and collaborates to manage project issues, proactively identify and mitigate risks and

drive milestone achievement.

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  • Tracks project deliverables against contract. Proactively prepares/presents study metrics to

maintain transparency for internal/external stakeholders. Monitors trends and drives changes

to the plan as needed; identifies risks to delivery and agrees to mitigation plans with the

project team to be presented to the client.

  • Ensures adherence to quality control expectations and milestone timelines for delivery of

contractually required reports and deliverables.

  • Identifies and manages changes to scope and requests for out-of-scope activities.

Collaborates with Business Development, Contracts Department, and executive management

to ensure timely execution of contract amendments/change orders. Prospectively manages

client expectations.

  • Supports development of Requests for Proposal (RFPs) for biopharma clients in collaboration

with leaders and key subject matter experts (SMEs).

  • Models and propagates Emmes’ commitment to a culture of quality in all aspects of our

deliverables, utilizing a solution-based, science-driven, value-added approach in collaborating

with clients.

  • Supports internal stakeholders on departmental initiatives upon request.
  • Contributes to the development and maintenance Ophthalmic Certification Project

Management SOPs and processes in collaboration with department leads.

  • Supports the identification and implementation of tools and process integrations that support

the efficiency and productivity of the OCPMG. This may include but is not limited to

collaboration with internal stakeholders and vendors to support global, OCPMG efficiency and

standardization within the department.

  • Performs other duties as assigned.

Qualifications

Travel

May travel between corporate locations.

Required Education And Experience

  • Bachelor’s degree or equivalent experience.
  • Minimum 6 years demonstrating related experience, with 3 years working in a pharmaceutical and/or Clinical Research Organization (CRO) setting. 2 years of related supervisory experience.

Required Skills/Abilities

  • Demonstrated experience with MS Office Suite, particularly MS Word.
  • Time management and decision-making skills.
  • Attention to detail and the ability to address several assignments simultaneously.
  • Excellent oral and written communication skills.
  • Some knowledge of clinical trials in ophthalmology preferred.

Required Job Behaviors

  • Collaboration: Contributes outstanding teamwork in the achievement of group and

corporate goals.

  • Initiative: Exhibits resourcefulness and action in making independent sound decisions.
  • Results-Oriented: Performs beyond current job to meet critical deadlines and deliverables.
  • Service-Oriented: Provides inspired service to internal/external clients that goes beyond

the expected.

  • Responsibility: Takes ownership of a situation and significantly improves processes and/or

service.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

  • Flexible Approved Time Off
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Research
Spoken language(s):
English
Check out the description to know which languages are mandatory.

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