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Immediate Need for a Clinical Trial Manager

Responsibilities:

• Manage clinical site interactions (including assistance with IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and supply requests, issue resolution, etc.)

• Manage trial start-up, conduct, and close-out activities according to industry and corporate standards with Director support

• Prepare key clinical documents (e.g. protocols, informed consent, amendments, CRFs, training materials, project plans, monitoring plans, data plans, statistical analysis plans, summary reports, annual reports, etc.)

• Establish professional rapport and maintain frequent communication with investigational site personnel to keep study on track

• Track internal metrics, timelines, and budgets

• Communicate trial status to the trial team

• Prepare and present trial-specific updates to the Director, Program Managers, and Senior Management

• Participate in monitoring activities at clinical trial sites to assure adherence to GCP and ICH guidelines, regulatory requirements, SOPs, and protocols and ensure that data is complete and accurate

• In conjunction with data management personnel, gain understanding of planning, monitoring, and executing data analyses

• Support applications and technical files as needed

• Collaborate with project-specific committees (e.g., DSMB, CEC)

• Assist in preparation for investigators' meetings

• Work with vendors as needed

• Travel up to 25% of the time

Experience Level

Intermediate Level

Pay and Benefits

The pay range for this position is $65.00 - $70.00/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 Andover,MA.

Application Deadline

This position is anticipated to close on May 29, 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 [email protected] (%[email protected]) for other accommodation options.