Sr. Study Manager, Oncology Job

Employer
Location
Gwynedd, PA, US
Posted
March 16 2017
Organization Type
Pharma
Sr. Study Manager, Oncology-CLI005740

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Duties and responsibilities include, but are not limited to the following:

- Accountable for the operational planning, feasibility, and execution of a clinical protocol.May lead team in key study planning, development and execution elements (e.g., data management deliverables, protocol level plans/timelines, country/site selection, system updates, Investigator Meeting planning, communication plans, preparation of status update reports, study closeout activities).
- May serve as the clinical trial team (CTT) lead.Leads team for timeline management, risk identification and mitigation, issue resolution.
- May facilitate and collaborate with key internal/external stakeholders (study team, subsidiary country teams, vendors, committees, etc) in support of clinical study objectives.
- Accountable for managing any study specific partners and/or vendors.

Qualifications

Education:

- Bachelor’s degree with a minimum of 11 years’ experience in clinical development; OR
- Bachelor’s degree in Life Science with a minimum of 7 years’ experience in clinical development; OR
- MS in Life Sciences with a minimum of 5 years’ experience in clinical development; OR
- PhD in Life Sciences with a minimum of 2 years’ experience in clinical development

Required:

- Pharmaceutical and/or clinical drug development experience.
- Excellent oral (including presentation) and written communication, computer/ database management and project management skills.

Preferred:

- Experience in study planning, conduct and management of oncology studies - specifically first-in-human / Phase Ib experience.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Clinical Research - Clin Ops

Job Title:Sr. Scientist, Clinical Operations

Primary Location: NA-US-PA-Upper Gwynedd

Other Locations: NA-US-NJ-Rahway

Employee Status: Regular

Travel: Yes, 15 % of the Time

Number of Openings: 3

Company Trade Name:Merck