Principal Clinical Data Manager - US/Europe - Remote
What the Data Management Department does at Worldwide
Our Data Management team is an ever-growing and collaborative group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies - from crafting the study database to ensuring the pristine delivery of the final dataset. We meticulously ensure data accuracy and integrity, crucial for groundbreaking regulatory submissions.
With a variety of roles, from data support staff, database and SAS programmers, coders, and functional leads, there are many opportunities to launch and further your career. Our team embraces an environment that invites input, fosters personal growth, and empowers your professional journey.
What you will do
• Oversee, lead, manage and provide technical expertise within the assigned complex projects/programs to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor's satisfaction. Provide subject matter expert support, solution management and departmental support for project initiatives and training.
• Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs
• Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings).
• Collaborate with internal WCT departments working on the same project .
• Provide mentorship to other members of the DM department.
• Participate in and co-lead departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadership.
• Deputise for Manager, DM as required.
• To provide support to Business Development staff by participating in preparation of proposals and presentations to sponsors.
• To participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings.
What you will bring to the role
• Excellent attention to detail.
• Excellent written and verbal communication skills.
• Expert knowledge of data management best practices & technologies as applied to clinical trials.
• Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
• Advanced understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
• Strong independent analytical and problem solving skills.
• Independent and autonomous project oversight skills.
Your experience
• Bachelor's degree or higher in biomedical sciences, life sciences, computer science or related discipline - or equivalent relevant experience.
• Min of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $99,000.00 - $196,000.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Our Data Management team is an ever-growing and collaborative group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies - from crafting the study database to ensuring the pristine delivery of the final dataset. We meticulously ensure data accuracy and integrity, crucial for groundbreaking regulatory submissions.
With a variety of roles, from data support staff, database and SAS programmers, coders, and functional leads, there are many opportunities to launch and further your career. Our team embraces an environment that invites input, fosters personal growth, and empowers your professional journey.
What you will do
• Oversee, lead, manage and provide technical expertise within the assigned complex projects/programs to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor's satisfaction. Provide subject matter expert support, solution management and departmental support for project initiatives and training.
• Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs
• Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings).
• Collaborate with internal WCT departments working on the same project .
• Provide mentorship to other members of the DM department.
• Participate in and co-lead departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadership.
• Deputise for Manager, DM as required.
• To provide support to Business Development staff by participating in preparation of proposals and presentations to sponsors.
• To participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings.
What you will bring to the role
• Excellent attention to detail.
• Excellent written and verbal communication skills.
• Expert knowledge of data management best practices & technologies as applied to clinical trials.
• Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
• Advanced understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
• Strong independent analytical and problem solving skills.
• Independent and autonomous project oversight skills.
Your experience
• Bachelor's degree or higher in biomedical sciences, life sciences, computer science or related discipline - or equivalent relevant experience.
• Min of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $99,000.00 - $196,000.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.