Worldwide Clinical Trials

Manager, Clinical Data Management

Worldwide Clinical Trials • $99K — $196K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in biomedical sciences, life sciences, computer science, or related field.
  • Minimum of 9 years in clinical data management or related role in pharmaceuticals, biotechnology, or medical devices.
  • 2-4 years of line management experience.
  • Expert knowledge of data management best practices in clinical trials.
  • Strong project management skills with experience in operational and budget oversight.

Responsibilities

  • Provide management and leadership oversight for teams and projects in Data Management.
  • Act as the primary contact for study-specific escalations.
  • Represent the company at sponsor governance meetings.
  • Manage departmental personnel, ensuring appropriate project allocation and oversight.
  • Define and monitor objectives for team members, promoting career development.
  • Support Business Development by preparing proposals and presentations.
  • Lead departmental initiatives for process improvement and efficiencies.

Benefits

  • Comprehensive benefits package depending on location.
  • Commitment to fostering an inclusive and equitable workplace.
  • Transparent compensation practices.
  • Opportunities for career and personal development.
  • Supportive environment for mentorship and training.
Full Job Description

SUMMARY:To provide management and leadership oversight of assigned teams and projects within Data Management department for study execution and budget management. Support development and implementation of Worldwide processes and initiatives.

RESPONSIBILITIES:

Tasks may include but are not limited to:

  • Provide management and leadership oversight of teams and projects within Data Management department for study execution and budget management. 

  • To act as the primary point of contact for any study specific escalations (internal or external).

  • Torepresentthe company at sponsor governance meetings.

  • Manage assigned departmental personnel ensuring:

  • staff areallocatedto projects appropriatelyand according to their abilities/competencies

  • appropriate oversight,trainingand mentoring is provided

  • projects within the team are appropriately resourced

  • operational or budget risks are discussed and addressed

  • any performance related escalations for team member are managed and handled appropriately

  • highlight upcoming availability to DM Management to ensure continuity of utilisation

  • Define andmonitorobjectives for individual team members, ensuring there are opportunities for career and personal development.

  • Provide support to Business Development staff byparticipatingin preparation of proposals and presentations to sponsors.​

  • Participate as necessary in sponsor audits, regulatory authority inspections and otherthird partymeetings. Ensure than any recommendations are discussed and that solutions are incorporated.​

  • As required, perform the role of Subject Matter Expert for a specific DM process:

  • Ongoing review to ensure the process is effective and efficient.

  • Central pointof contact for any related questions from the team.

  • Provide ongoing training to all team members.

  • Take ownership of any related Quality Issuesidentified, ensuring root cause analysis and CAPAs asrequired.

  • Ownership and regular updates of related QMDs or other guidance documents.

  • Provide mentorship to other members of the DM department.

  • Lead and manage departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadership.

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

OTHER SKILLS AND ABILITIES:

  • 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.

  • Independent analytical andproblem solvingskills.

  • Strong project management skills and experience managing data management teams and projects for operational and budget oversight

  • Line management experience including recruitment, careerdevelopmentand performance reviews.

REQUIREMENTS: 

  • Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience. 

  • Min of 9 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. 

  • 2-4 years of line management experience. 

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility taken, and ability to work independently. 

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. 

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

Similar Jobs

More Jobs at Worldwide Clinical Trials

More Pharmaceuticals & Biotech Jobs

Find similar Manager, Clinical Data Management jobs: