Associate Director Of Clinical Data Management

Job Title: Associate Director of Clinical Data Management

Job Description

As an Associate Director of Clinical Data Management, you will lead and oversee a team within Clinical Data Management, ensuring the successful execution of data management deliverables for large, complex clinical trials or programs involving multiple trials. You will be responsible for developing data management strategies, managing vendors, reviewing contracts, and ensuring compliance with SOPs and regulatory guidelines. You will also act as the main point of communication for internal discussions, escalations, and stakeholder management concerning data management topics.

Responsibilities

• Mentor and guide the Clinical Data Management (CDM) team, aligning with strategic goals.
• Develop and implement strategies for maintaining high-quality data from database build through cleaning and review.
• Represent CDM in program and study meetings, influencing resourcing decisions.
• Serve as the senior CDM representative on multi-disciplinary teams, ensuring alignment on CDM activities.
• Lead initiatives to streamline operations and sponsor department-level improvements.
• Manage key data management activities using project management methodologies.
• Manage relationships and alignment with cross-functional stakeholders and leadership.
• Oversee data management vendors, ensuring that their delivery meets expectations.

Essential Skills

• Proficiency in data management and EDC systems such as Medidata RAVE.
• Strong vendor management skills.
• Experience with database lock processes.
• Knowledge of oncology data and clinical trial processes.
• Expertise in CRF design and clinical data management.
• Bachelor’s or Master’s degree in Life Sciences, Statistics, Informatics, Computer Sciences, or equivalent experience.
• At least 12 years of directly relevant work experience.
• Experience as a Clinical Data Manager in pharma/biotech or CRO.
• Demonstrated leadership in DM technical responsibilities and systems.
• Skilled in negotiating solutions with cross-functional teams.
• Strong communication skills, especially with senior stakeholders.
• Experience managing CROs and DM-related vendors.
• Understanding of regulatory guidelines and industry standards such as ICH/FDA, CDISC, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries.
• Knowledge of Phase 1–4 clinical studies and core DM tasks.
• Excellent project management and multitasking skills.
• Attention to detail and ability to work independently or in teams, including with external partners/vendors.

Additional Skills & Qualifications

• Oncology and Phase III/Pivotal study experience preferred.
• Strong technical skills and experience with various DM systems.

Work Environment

The role requires working on-site in Conshohocken, PA, three days a week up to five.

Job Type & Location

This is a Contract position based out of Conshohocken, Pennsylvania.

Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for more information.

Pay and Benefits

The pay range for this position is $80.00 - $96.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Conshohocken,PA.

Application Deadline

This position is anticipated to close on Oct 20, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $80 - $96