Job Opportunities in Costa Rica

Introducing Global Clinical Data Integration (GCDI): Transforming clinical data management in Latin America. With a focus on streamlining information, our department collects, cleans, transforms, and archives clinical data, ensuring high quality and compliance. As a new addition to the region, we intend to enhance efficiency and leverage local information across departments to drive innovation and deliver value across clinical trials, data management standards, and technology platforms.

Are you passionate about revolutionizing clinical data management and making a difference in drug and vaccine programs? As a Technical Project Manager, you will oversee the end-to-end management and delivery of technical solutions for clinical trials, ensuring they are executed with precision and quality. Your role will encompass everything from the development and management of technical project plans to the seamless deployment of technical deliverables. Join us and be a key player in our mission to advance healthcare through innovative data management.

If you’re an experienced and detail-oriented individual with a strong background in clinical data management and technology implementation, this is your chance to make an impact. Click "Apply" now to become a part of a dynamic team where your expertise will contribute to the success of groundbreaking clinical trials. Embrace this exciting opportunity to lead and innovate within a transformative field.

Main Requirements:

• Bachelor’s degree in life sciences, computer science, or a related discipline.
• Minimum of 2 years of experience in Data Management and overall 5 years in software development, programming or technology implementation.
• Experience with project management tools such as Microsoft Project; PM certifications are a plus.
• Proficiency in database development and validation activities.
• Previous experience with software implementation will be considered a plus.
• Understanding of the clinical research process and in-depth knowledge of the Clinical Data Management lifecycle will be considered a plus.
• Strong organizational and leadership abilities.
• Effective communication skills in both oral and written forms, in English and Spanish, with the capability to engage technical and business stakeholders.
• Ability to thrive in a complex, fast-paced environment with a customer-focused mindset.
• Demonstrated ability to work collaboratively with cross-functional teams, adapting to different working styles and personalities to achieve project goals.
• Proven skills in conflict resolution and influential leadership, capable of navigating and negotiating with stakeholders at all organizational levels to ensure timely and successful project completion.

Job Responsibilities:

• Develop and manage detailed technical project plans for clinical trials, covering design, testing, deployment, and maintenance of technical deliverables such as e CRFs, data collection systems, and system integrations.
• Define trial-level technical requirements by collaborating with key stakeholders and subject matter experts to ensure quality data collection and validation.
• Ensure timely and high-quality delivery of all technical data management components, monitoring their status and addressing any change requests as necessary.
• Coordinate the decommissioning of clinical data management technologies post-trial.
• Utilize excellent project management skills under the guidance of senior staff, including project planning, resource coordination, risk management, and stakeholder communication.
• Provide technical support during audits and contribute to the continuous improvement of data collection and management processes.

Take the next step in your career and join us in delivering cutting-edge technical solutions for clinical trials. Apply now and be part of a team dedicated to advancing clinical data integration and healthcare innovation.

Data Integration Latam
Data Integration CR

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
11/2/2024

• A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
  

Requisition ID:R317003