Lead Clinical Data Manager - Remote North America

PPD
Wilmington, NC Remote Full Time
POSTED ON 12/7/2022 CLOSED ON 3/17/2023

What are the responsibilities and job description for the Lead Clinical Data Manager - Remote North America position at PPD?

Remote North America
Full-Time Regular w/ Benefits
FSP and Full Service Opportunities Available!

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.

Are you a data and a people person? Here’s your team. We manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust.

As a Clinical Data Team Lead, you will help ensure the highest quality of data and effectiveness of clinical trail data. You will work directly with Senior Clinical Data Team Leads to create, monitor and close studies in a timely manner. This position also works with sites, clients, and other team members at PPD.

At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.

Summarized Purpose:
Acts as the lead data manager for one or more projects or to provide support to the lead data manager. May lead all data management activities for individual, limited volume/complexity studies with support from senior team members. Acts as an interdepartmental and client liaison for all DM study activities.

Essential Functions:

  • Applies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks.

  • Acts as a liaison to the PM and/or client as required and communicates with management regarding all data management (DM) activities within their studies.

  • Develops and maintains data management project documentation files; performs independent reviews of data management deliverables following documented CDM guidelines.

  • Develops and delivers study specific training for DM project staff.

  • Produces project-specific status reports for management, PM and/or clients on a regular basis. Monitors study metrics.

  • May participate in business development activities by assisting with bid preparation and/or representing data management at bid defense meetings, where required. Assists with project forecasting of hours and identification of resource requirements and identifies potential out of scope activities to Project Managers and management and assists with the Contract Modification process.

  • May mentor junior level staff on all associated tasks within a study.

  • Assists with the administrative and financial management of allocated projects. Performs all assigned data management activities independently and efficiently, with attention to quality.


Education/Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years). Addtional experience required for Senior Clinical Data Team Lead.


Qualified candidates should have prior expereince in Clinical Data Management or Clinical operations, preferably with a CRO, Pharma, Biotech or relevant industry.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills & Abilities:

  • Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations

  • Ability to use interactive computer programs

  • Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail

  • Ability to work productively with minimal supervision

  • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data

  • Strong customer focus and excellent interpersonal skills

  • Proven flexibility and adaptability

  • Ability to work in a team environment and independently as needed

  • Ability to train and direct study team

  • Ability to set and meet timelines or be able to recognize and schedule changes in response to project demands

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 and 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. 10-20% annual possible.

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