Mgr CDM Study Lead

BioSpace; New Jersey; On-site; USD 114,800 - 187,400; Full time

Benefits offered by this job

Health and wellness programs

401(k) company match

Annual bonuses

Paid time off and paid leaves

Job summary

A leading biotechnology company based in New Jersey is seeking a Manager, Clinical Data Management to oversee clinical data management projects across various therapeutic areas. The ideal candidate will have at least 8 years of experience in clinical data management within biotech or pharmaceutical industries. Responsibilities include supervising teams, managing data quality, and ensuring compliance with regulatory standards. This position offers competitive benefits, emphasizing collaborative work onsite.

Qualifications

• 8+ years of clinical data management experience in biotech, pharmaceutical, or health-related industry.
• Experience in oncology or ophthalmology is a plus.
• Ability to work independently within tight timelines.

Responsibilities

• Oversee lead Data Manager(s) on assigned clinical data management projects.
• Supervise direct reports for timely and quality results.
• Ensure databases are developed and validated in compliance with regulations.

Skills

Clinical data management

Leadership

Communication

Attention to detail

Education

Bachelor's degree in mathematics, Science or related field

Tools

CDMS

EDC applications

Microsoft Office

Job description

Overview

The Manager, Clinical Data Management provides oversight of lead Data Manager(s) on assigned clinical data management projects in multiple therapeutic areas to assure proper planning and execution for data management results that meet Regeneron standards and within timelines.

Typical Day Might Include

• Serves as primary DM contact for assigned therapeutic areas to interact with clinical counterparts for overall project planning and issue resolution. Projects, allocates and prioritizes DM resources within the assigned therapeutic projects.
• Supervises direct DM reports for planning and managing all relevant DM activities within the assigned therapeutic areas for timely and quality results and within the budget. Mentor junior data managers for skills advancement. If required, leads and performs clinical data management tasks for studies.
• Supervises and ensures all databases are developed, validated and ready for transfer and/or analysis according to policies and procedures, SOPs and work instructions in compliance with applicable regulations.
• Reviews and approves for final archival of project documentation, including, but not limited to, Data Management Manual, CRF Completion Guidelines and validation specifications, and work instructions for assigned projects. Designs and modifies CRF.

This Role Might Be For You If

• Supervises DM direct reports for the initiation and approval of the building, and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Coordinates with clinical project team for issue resolution.
• Contributes to development of Regeneron DM outsourcing strategies and long‑term relationships with outsourcing partners with objective of ensuring data quality and efficiencies through data and process standardization.
• Ensures adequate management of CROs and vendors in the therapeutic projects and coordinates all data management functions.
• Establishes goals, expectations and accountabilities for direct reports. Regularly reviews DM performance in respect to quality and timeliness standards according to Regeneron SOPs and working procedures. Responsible for coaching, handling training and leading the direct reports.

To be considered

• Bachelors degree in mathematics, Science or a related field, along with at least 8 or more years of clinical data management experience in biotech, pharmaceutical or health related industry. Previous oncology and/or ophthalmology experience a plus. Previous managerial experience is preferred.
• Directed and comfortable working in teams with the ability to work and operate independently within a tight time line environment. High degree of creativity, latitude and attention to detail required.
• Knowledge of all applicable regulations including CFR, GCP, and ICH Guidelines. Strong communication, leadership and business development skills required.
• Proficient with appropriate EDC applications and Microsoft Office applications. Software proficiency with CDMS required. Experience with JMP and SAS a plus.

Apply Now

Does this sound like you? Apply now to take your first step towards living the Regeneron Way!

Benefits

We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries specific benefits, please speak to your recruiter.

On-site Policy

Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regenerons roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about Regenerons on‑site policy and expectations for your role and your location.

Equal Opportunity Employer

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.

Salary Range (annually)

$114,800.00 - $187,400.00

Salary Information

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Background Check

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.